EndaCof DM description, usages, side effects, indications, overdosage, supplying and lots more!

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EndaCof DM

Larken Laboratories, Inc.




FULL PRESCRIBING INFORMATION

Drug Facts

(In each 5 mL teaspoonful)

Brompheniramine Maleate, USP   1 mg

Dextromethorphan HBr, USP   5 mg

Phenylephrine HCl, USP   2.5 mg

Brompheniramine Maleate   Antihistamine

Dextromethorphan HBr        Antitussive (cough suppressant)

Phenylephrine HCl               Nasal decongestant

Temporarily relieves these symptoms due to hay fever (allergic rhinitis):

  • cough due to minor throat and bronchial irritation
  • runny nose
  • sneezing
  • itchy, watery eyes
  • itching of the nose or throat
  • temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies
  • temporarily restores freer breathing through the nose

Do not use

  • to sedate a child or make a child sleepy
  • if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this drug.
  • heart disease
  • high blood pressure
  • thyroid disease
  • diabetes
  • glaucoma
  • trouble urinating due to an enlarged prostate gland
  • a breathing problem such as emphysema or chronic bronchitis
  • a cough that lasts or is chronic such as occurs with smoking, asthma or emphysema
  • a cough that occurs with too much phlegm (mucus)
  • taking any other nasal decongestant or stimulant
  • taking sedatives or tranquilizers

Do not exceed recommended dosage.

  • marked drowsiness may occur
  • avoid alcoholic beverages
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • be careful when driving a motor vehicle or operating machinery
  • excitability may occur, especially in children
  • nervousness, dizziness, or sleeplessness occur.
  • cough or nasal congestion persists for more than 1 week, tends to recur, or is accompanied by a fever, rash or persistent headache. These could be signs of a serious condition.

ask a health professional before use.

In case of overdose, get medical help or contact a Poison Control Center immediately.

Do not exceed 6 doses in a 24-hour period

Age Dose
Adults and children over 12 years of age 4 teaspoonsful (20 mL) every 4 hours
Children 6 to under 12 years of age 2 teaspoonsful (10 mL) every 4 hours
Children under 6 years of age Ask your doctor
  • store at 20°-25°C (68°-77°F)
  • very low sodium, contains 1 mg sodium per teaspoonful (5 mL)

Benzoic acid, edetate disodium, FD&C Red #40, propylene glycol, purified water saccharin sodium, sorbitol solution and strawberry flavoring

Call 1-888-527-5522 weekdays from 9:00 am to 4:00 pm CST or go to http://www.larkenlabs.com.

Figure 1: 16 oz. Bottle Label

EndaCof DM

EndaCof DM

Brompheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68047-143
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Brompheniramine Maleate BROMPHENIRAMINE 1 mg
DEXTROMETHORPHAN HYDROBROMIDE DEXTROMETHORPHAN 5 mg
Phenylephrine Hydrochloride PHENYLEPHRINE 2.5 mg

Inactive Ingredients

Ingredient Name Strength
BENZOIC ACID
EDETATE DISODIUM
FD&C RED NO. 40
propylene glycol
water
SACCHARIN SODIUM DIHYDRATE
sorbitol

Product Characteristics

Color
RED

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68047-143-16 473 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2012-03-30


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Be sure to consult your doctor before taking any medication!
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