Wednesday, September 14, 2016

Poly Hist DHC



dihydrocodeine bitartrate, phenylephrine hydrochloride and pyrilamine maleate

Dosage Form: liquid
Poly Hist DHC

Poly Hist DHC Liquid


CIII

NDC 50991-521-16

Rx Only


DESCRIPTION:

Each 5 mL (one teaspoonful) for oral administration contains:

Dihydrocodeine Bitartrate*.......................... 7.5 mg

(*WARNING - May be habit forming)

Phenylephrine HCl.................................... 5 mg

Pyrilamine Maleate................................... 7.5 mg


Poly Hist DHC Liquid also contains: Citric Acid, Glycerin, Fruit Gum Flavor, Propylene Glycol,

Sorbitol, Purified Water, Sodium Citrate, Sodium Saccharin.


Dihydrocodeine Bitartrate is an antitussive with the chemical name (Morphinan-6-ol,4,5-epoxy-3-methoxy-17-methyl-,

(5α, 6α)-2,3-dihydroxybutanedioate (1:1) (salt) 4,5α-Epoxy-3-methoxy-17-methylmorphinan-6α-ol (+)-tartrate (salt).

It has the following structural formula:





Phenylephrine hydrochloride is an orally effective nasal decongestant. Chemically it is Benzenemethanol,

3-hydroxy-α-[(methylamino)methyl]-,hydrochloride (R)-, (-)-m-Hydroxy-α- [(methylamino)methyl]benzyl alcohol

hydrochloride. Its chemical structure is as follows:





Pyrilamine Maleate is an antihistamine having the chemical name 1,2-Ethanediamine, N-[(4-methoxyphenyl)methyl]-N',

N'-dimethyl-N-2-pyridinyl-, (Z)-2-butenedioate (1:1) 2-[[2-Dimethylamino)ethyl](p-methoxybenzyl)amino] pyridine

maleate (1:1); Its structural formula is as follows:




Poly Hist DHC - Clinical Pharmacology


Dihydrocodeine is a semi-synthetic narcotic analgesic related to codeine, with multiple actions

qualitatively similar to those of codeine; the most prominent of these involve the central nervous

system and organs with smooth muscle components.


Phenylephrine HCl is a sympathomimetic, which acts predominately on alpha-receptors and has little

action on beta-receptors. It therefore functions as an oral nasal decongestant with minimal CNS

stimulation.


Pyrilamine Maleate is an antihistamine used in suppressing symptoms of allergic rhinitis. However, it

is more prone to cause drowsiness than some other antihistamines.

Indications and Usage for Poly Hist DHC


Poly Hist DHC Liquid is indicated to control cough and provide for temporary relief from

congestion associated with the upper respiratory tract.

Contraindications


This combination product is contraindicated in patients with hypersensitivity to dihydrocodeine,

codeine, or any of the active and inactive components listed above, or in any situation where

opioids are contraindicated including significant respiratory depression (in unmonitored settings

or in the absence of resuscitation equipment), acute or severe bronchial asthma or hypercapnia,

and paralytic ileus. Antihistamines and sympathomimetics are contraindicated in patients receiving

antihypertensive or antidepressant drugs containing monoamine oxidase (MAO) inhibitors.

Antihistamines should not be used to treat lower respiratory tract symptoms or be given to

premature or newborn infants. Sympathomimetic agents are contraindicated in patients with

severe hypertension, severe coronary artery disease, patients with narrow angle glaucoma,

bronchial asthma, urinary retention, peptic ulcer, and during an asthma attack. This product is

contraindicated in women who are pregnant.

Warnings


General: Considerable caution should be exercised in patients with hypertension, diabetes mellitus,

ischemic heart disease, hyperthyroidism, increased intraocular pressure and prostatic hypertrophy.

The elderly (60 years and older) are more likely to exhibit adverse reactions. Antihistamines may

cause excitability, especially in children. At dosages higher than the recommended dose, nervousness,

dizziness, or sleeplessness may occur.


Usage in Ambulatory Patients: Dihydrocodeine may impair the mental and/or physical abilities

required for the performance of potentially hazardous tasks such as driving a car or operating machinery.


Respiratory Depression: Respiratory depression is the most dangerous acute reaction produced

by opioid agonist preparations, although it is rarely severe with usual doses. Opioids decrease the

respiratory rate, tidal volume, minute ventilation, and sensitivity to carbon dioxide. Respiratory

depression occurs most frequently in elderly more debilitated patients, usually after large initial doses

in non-tolerant patients, or when opioids are given in conjunction with other agents that depress

respiration. This combination product should be used with caution in patients with significant chronic

obstructive pulmonary disease or cor pulmonale and in patients with a substantially decreased

respiratory reserve, hypoxia hypercapnia, or respiratory depression.


Hypotensive Effect: Dihydrocodeine, like all opioid analgesics, may cause hypotension in patients

whose ability to maintain blood pressure has been compromised by a depleted blood volume or who

receive concurrent therapy with drugs such as phenothiazines or other agents which compromise

vasomotor tone. Poly Hist DHC Liquid may produce orthostatic hypotension in ambulatory patients.

This combination product should be administered with caution to patients in circulatory shock, since

vasodilation produced by the drug may further reduce cardiac output and blood pressure.


Dependence: Dihydrocodeine can produce drug dependence of the codeine type and has the

potential of being abused. This product should be prescribed and administered with the appropriate

degree of caution. (See Drug Abuse and Dependence section).

Precautions


General: This combination product should be used with caution in elderly or debilitated patients

or those with any of the following conditions: adrenocortical insufficiency (e.g., Addison's disease);

asthma; central nervous system depression or coma; chronic obstructive pulmonary disease;

decreased respiratory reserve (including emphysema, severe obesity, cor pulmonale, or

kyphoscoliosis); delirium tremens; diabetes; head injury; hypotension; hypertension; increased

intracranial pressure; myxedema or hypothyroidism; prostatic hypertrophy or urethral stricture; and

toxic psychosis. The benefits and risks of opioids in patients taking monoamine oxidase inhibitors

and in those with a history of drug abuse should be carefully considered. This combination product

may aggravate convulsions in patients with convulsive disorders, and like all opioids, may induce or

aggravate seizures in some clinical settings.

Drug Interactions


General: Sympathomimetics may reduce the antihypertensive effects of methyldopa,

mecamylamine, reserpine and veratrum alkaloids.


Other Central Nervous System Depressants: Patients receiving other opioid analgesics,

sedatives or hypnotics, muscle relaxants, general anesthetics, centrally acting anti-emetics,

phenothiazines or other tranquilizers, or alcohol concomitantly with this combination product

may exhibit additive depressant effects on the central nervous system. When such combined

therapy is contemplated, the dose of one or both agents should be reduced. Concomitant use

of dihydrocodeine and antihistamines with alcohol and other CNS depressants may have an

additive effect.


Monoamine Oxidase Inhibitors: Dihydrocodeine, like all opioids, interact with monoamine

oxidase inhibitors causing central nervous system excitation and hypertension. MAO inhibitors

and beta-adrenergic blockers increase the effects of sympathomimetics. They may also prolong

and intensify the anticholinergic effects of antihistamines.

Information for Patient/Caregivers:


Patients receiving Poly Hist DHC Liquid should be given the following information:

1. Patients should be advised that Poly Hist DHC Liquid may impair the mental or

    physical abilities required for the performance of potentially hazardous tasks such

    as driving a car or operating machinery.

2. Patients should be advised to report adverse experiences occurring during therapy.

3. Patients should be advised not to adjust the dose of Poly Hist DHC Liquid without

    consulting the prescribing professional.

4. Patients should not combine Poly Hist DHC Liquid with alcohol or other central

    nervous system stimulants.

5. Women of childbearing potential who become, or are planning to become pregnant

    should be advised to consult their physician regarding the effects of opioids and other

    drug use during pregnancy on themselves and their unborn child.


Patients should be advised that Poly Hist DHC Liquid is a potential drug of abuse. They

should protect if from theft, and it should never be given to anyone other than the individual

for whom it was prescribed.


Pregnancy: Teratogenic Effects - Pregnancy Category C:


Animal reproduction studies have not been conducted with Poly Hist DHC Liquid. It is also

not known whether this combination product can cause fetal harm when administered to

pregnant women or can affect reproduction capacity in males and females. This combination

product should be given to pregnant women only if clearly needed, especially during the first

trimester.

Nonteratogenic Effects:


Babies born to mothers who have been taking opioids regularly prior to delivery will be

physically dependent. The withdrawal signs include irritability and excessive crying, tremors,

hyperactive reflexes, increased respiratory rate, increased stools, sneezing, yawning,

vomiting and fever. The intensity of the syndrome does not always correlate with the duration

of maternal opioid use or dose. There is no consensus on the best method of managing

withdrawal. Chlorpromazine 0.7-1.0 mg/kg q6h, phenobarbital 2 mg/kg q6h, and paregoric

24 drops/kg q4h, have been used to treat withdrawal symptoms in infants. The duration of

therapy is 4 to 28 days, with the dosages decreased as tolerated.

Labor and Delivery:


Poly Hist DHC Liquid is not recommended for use by women during and immediately

before labor and delivery because oral opioids may cause respiratory depression in the

newborn.

Pediatric Use:


This product is not recommended for use in children under 6 years of age. Children under two

years may be more susceptible to the respiratory arrest, coma and death. Use of antihistamines

is not recommended in infants. This age group may be at a higher risk than other age groups

because of an increased susceptibility to anticholinergic effects, such as CNS excitation, and an

increased tendency toward convulsions. In older children taking antihistamines, a paradoxical

reaction characterized by hyperexcitability may occur. Very young children may be more sensitive

to the effects, especially the vasopressor effects of sympathomimetic amines.

Geriatric Use:


Poly Hist DHC Liquid should be given with caution to the elderly.


Hepatic Impairment:

POLYHIST DHC Liquid should be given with caution to patients with hepatic insufficiency.

Since, dihydrocodeine is metabolized by the liver; the effects of this combination

product should be monitored closely in such patients.


Renal Impairment:

Poly Hist DHC Liquid should be used with caution and in reduced dosage in the

presence of impaired renal function.


Pancreatic/Biliary Tract Disease:

Opioids may cause spasms of the sphincter of Oddi and should be used with caution in

patients with biliary tract disease including pancreatitis.

Adverse Reactions


The most frequently observed adverse reactions with dihydrocodeine include light-headedness,

dizziness, drowsiness, headache, fatigue, sedation, sweating, nausea, vomiting, constipation,

pruritis, and skin reactions. With the exception of constipation, tolerance develops to most of

these effects. Other reactions that have been observed with dihydrocodeine or other opioids

include respiratory depression, orthostatic hypotension, cough suppression, confusion, diarrhea,

miosis, abdominal pain, dry mouth, indigestion, anorexia, spasm of biliary tract, and urinary

retention. Physical and psychological dependence are possibilities. Hypersensitivity reactions

(including anaphylactoid reactions), hallucinations, vivid dreams, granulomatous interstitial nephritis,

severe narcosis and acute renal failure have been reported rarely during dihydrocodeine administration.

Other adverse reactions observed with the ingredients in Poly Hist DHC Liquid include, lassitude,

nausea, giddiness, dryness of mouth, blurred vision, cardiac palpitations, flushing, increased irritability

or excitement (especially in children).

Drug Abuse and Dependence


This combination product is subject to the provisions of the Controlled Substance Act and

has been placed in Schedule III. Dihydrocodeine can produce drug dependence of the codeine

type and therefore has the potential of being abused. Psychological dependence, physical

dependence, and tolerance may develop upon repeated administration of dihydrocodeine, and

it should be prescribed and administered with the same degree of caution appropriate to the

use of other oral opioid medications. Symptoms of dihydrocodeine withdrawal consist of

irritability, restlessness, insomnia, diaphoresis, anxiety and palpitations.

Overdosage


An overdose of Poly Hist DHC Liquid is a potentially lethal poly-drug overdose situation,

and consultation with a regional Poison Control Center is recommended. A listing of the

poison control centers can be found in standard references such as the Physician's Desk

Reference®.


Signs and Symptoms: Symptoms of overdosage include pinpoint pupils, respiratory depression,

extreme somnolence progressing to stupor, loss of consciousness, or coma, skeletal muscle

flaccidity, cold and clammy skin and other symptoms common with narcotic overdosage.

Convulsions, cardiovascular collapse, and death may occur. A single case of acute

rhabdomyolysis associated with an overdose of dihydrocodeine has been reported.


Recommended Treatment: Immediate treatment of an overdosage of Poly Hist DHC

Liquid includes support of cardiorespiratory function and measures to reduce drug absorption.

Vomiting should be induced with syrup of ipecac, if the patient is alert and has adequate laryngeal

reflexes. Oral activated charcoal should follow. The first dose should be accompanied by an

appropriate cathartic. Gastric lavage may be necessary. Hypotension is usually hypovolemic and

should be treated with fluids. Endotracheal intubation and artificial respiration may be necessary.

The pure opioid antagonist naloxone or nalmefene is a specific antidote against respiratory depression

that results from opioid overdose. Opioid antagonists should not be given in the absence of clinically

significant respiratory or circulatory depression secondary to opioid overdose. They should be

administered cautiously to persons who are known, or suspected to be, physically dependent on any

opioid agonist including dihydrocodeine. In such cases, an abrupt or complete reversal of opioid

effects may precipitate an acute abstinence syndrome. The prescribing information for the specific

opioid antagonist should be consulted for details of their proper use.

DOSAGE AND ADMINISTRATION*


Adults and Children 12 years of age and older:

1 teaspoonful every 4 to 6 hours. Not to exceed 6 teaspoonfuls in a 24 hour period.

Children 6 to 12 years of age:

1/2 teaspoonful every 4 to 6 hours. Not to exceed 3 teaspoonfuls in a 24 hour period.

Not recommended for children under 6 years of age.


*In mild cases or in particularly sensitive patients, less frequent or reduced doses

may be appropriate and adequate.

How is Poly Hist DHC Supplied


Poly Hist DHC is supplied as an alcohol free, gluten free, sugar free, fruit gum flavor,

clear colored liquid supplied in 16 oz. bottles (NDC 50991-521-16) and 15 mL professional

sample (NDC 50991-521-15).


KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

IN CASE OF ACCIDENTAL OVERDOSE, SEEK PROFESSIONAL ASSISTANCE

OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.


Tamper evident by foil seal under cap. Do not use if foil seal is broken or missing.

Storage:


Store at 20o-25oC (68o-77oF); excursions permitted to 15o-30oC (59o-86oF).

[See USP Controlled Room Temperature.] Protect from freezing.


Dispense in a tight, light-resistant container as defined in the USP/NF with a child-resistant closure.


This bottle not to be dispensed to consumer.


Rx only


Manufactured by:

Great Southern Laboratories

Houston, TX 77099


Distributed for:

Poly Pharmaceuticals

Mobile, AL 36619


Rev. 09/09

PRODUCT PACKAGING:


The packaging below represents the labeling currently used:


Principal Display Panel and Side Panel for 473mL Label:


NDC 50991-521-16


Poly Hist DHC


Antitussive / Decongestant / Antihistamine


Each 5 mL (1 teaspoonful) contains:

Dihydrocodeine Bitartrate*....... 7.5 mg

*(WARNING: May be habit forming)

Phenylephrine HCl....................  5 mg

Pyrilamine Maleate................. 7.5 mg


Fruit Gum Flavor

Alcohol Free / Gluten Free

Sugar Free / Dye Free


CIII

Rx Only


Distributed by:

Poly Pharmaceuticals

Mobile, AL 36619


16 fl oz. (473 mL)




Side Panel:


DOSAGE AND ADMINISTRATION*: Adults and Children 12 years of age and older:

1 teaspoonful every 4 to 6 hours. Not to exceed 6 teaspoonfuls in a 24 hour period.

Children 6 to 12 years of age: 1/2 teaspoonful every 4 to 6 hours. Not to exceed 3

teaspoonfuls in a 24 hour period.

Not recommended for children under 6 years of age.


*In mild cases or in particularly sensitive patients, less frequent or reduced doses may be

appropriate and adequate.


Refer to the attached package insert for full prescribing information.


KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

IN CASE OF ACCIDENTAL OVERDOSE, SEEK PROFESSIONAL ASSISTANCE

OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.


Tamper evident by foil seal under cap. Do not use if foil seal is broken or missing.


This bottle is not to be dispensed to consumer.


Storage: Store at 20o-25oC (68o-77oF); excursions permitted to 15o-30oC (59o-86oF).

[See USP Controlled Room Temperature.] Protect from freezing.


Dispense in a tight, light-resistant container with a child-resistant cap.


Rx Only


Manufactured by: Great Southern Laboratories, Houston, TX 77099


Distributed for: Poly Pharmaceuticals, Mobile, AL 36619


Iss. 09/09












POLY HIST  DHC
dihydrocodeine bitartrate, phenylephrine hydrochloride, pyrilamine maleate  liquid










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)50991-521
Route of AdministrationORALDEA ScheduleCIII    














Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Dihydrocodeine Bitartrate (Dihydrocodeine)Dihydrocodeine Bitartrate7.5 mg  in 5 mL
Phenylephrine Hydrochloride (Phenylephrine)Phenylephrine Hydrochloride5 mg  in 5 mL
Pyrilamine Maleate (Pyrilamine)Pyrilamine Maleate7.5 mg  in 5 mL





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
Color    Score    
ShapeSize
FlavorBUBBLE GUMImprint Code
Contains      










Packaging
#NDCPackage DescriptionMultilevel Packaging
150991-521-16473 mL In 1 BOTTLENone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved other11/12/2009


Labeler - Poly Pharmaceuticals, Inc. (198449894)

Registrant - Great Southern Laboratories (056139553)









Establishment
NameAddressID/FEIOperations
Great Southern Laboratories056139553manufacture
Revised: 11/2009Poly Pharmaceuticals, Inc.

More Poly Hist DHC resources


  • Poly Hist DHC Side Effects (in more detail)
  • Poly Hist DHC Dosage
  • Poly Hist DHC Use in Pregnancy & Breastfeeding
  • Poly Hist DHC Drug Interactions
  • 0 Reviews · Be the first to review/rate this drug


  • Poly Hist DHC Liquid MedFacts Consumer Leaflet (Wolters Kluwer)


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