ABATUSS DMX description, usages, side effects, indications, overdosage, supplying and lots more!

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ABATUSS DMX

Kramer Novis

ABATUSS DMX Antihistamine Cough Suppressant Nasal Decongestant GRAPE Flavor


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients(in each 5 mL teaspoonful)

Dexchlorpheniramine maleate, USP 1 mg
Dextromethorphan HBr, USP 15 mg
Pseudoephedrine HCl, USP 30 mg

Purpose

Antihistamine
Cough suppressant
Nasal Decongestant

ABATUSS DMX Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

  • sneezing
  • itchy nose or throat
  • runny nose
  • itchy, watery eyes
  • nasal congestion
  • temporarily controls cough due to minor throat and bronchial irritation associated with inhaled irritants
  • temporarily restores freer breathing through the nose

Warnings


Do not use 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 product.

Ask a doctor before use if

you have

  • heart disease
  • high blood pressure
  • thyroid disease
  • diabetes
  • glaucoma
  • cough that occurs with too much phlegm (mucus)
  • trouble urinating due to an enlarged prostrate gland
  • a breathing problem or chronic cough that lasts or occurs with smoking, asthman, chronic bronchitis or emphysema

Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers


When using this product

  • do not exceed recommended dosage
  • excitability may occur especially in children
  • marked drowsiness may occur
  • alcohol, sedatives, and tranquilizers may increase the drowsiness effect
  • avoid alcoholic beverages while taking this product
  • do not take this product if you are taking sedatives or tranquilizers, without first consulting your doctor
  • use caution when driving a motor vehicle or operating machinery

Stop use and ask a doctor if

  • nervousness, dizziness, or sleeplessness occur
  • new symtoms occur
  • symptoms do not improve within 7 days or are accompanied by fever
  • cough lasts for more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious conditions.

If pregnant or breastfeeding

ask a health professional before use.

Keep out of reach of children.

In case of accidental overdose, get medical help or contact a Poison Control Center right away.

Directions


  • do not take more than 4 doses in any 24-hour period
  • EVERY 6 HOURS
Adults and children 12 years of age and older:
10 mL (2 tsp)
Children 6 to under 12 years of age:
5 mL (1 tsp)
Children 2 to under 6 years of age:
consult a physician

ABATUSS DMX Other information

  • Store at room temperature 15°C-30°C (59°F-86°F)
  • protect from freezing
  • protect from light
  • Avoid excessive heat or humidity
  • TAMPER EVIDENT: Do not use this product if breakaway band on cap is broken on missing

Inactive ingredients

Art. Flavor, Citric Acid, D&C Red #33, FD&C Blue #1, Glycerin, Sodium benzoate, Sodium saccharin, Sorbitol, Water

ABATUSS DMX Cough Suppressant Nasal Decongestant Antihistamine GRAPE Flavor

ABATUSS DMX

ABATUSS DMX

DEXCHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PSEUDOEPHEDRINE HYDROCHLORIDE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52083-625
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Dexchlorpheniramine Maleate DEXCHLORPHENIRAMINE 1 mg
DEXTROMETHORPHAN HYDROBROMIDE DEXTROMETHORPHAN 15 mg
Pseudoephedrine Hydrochloride Pseudoephedrine 30 mg

Inactive Ingredients

Ingredient Name Strength
CITRIC ACID MONOHYDRATE
FD&C BLUE NO. 1
D&C RED NO. 33
GLYCERIN
SODIUM BENZOATE
water
sorbitol
saccharin sodium

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 473 in 1 BOTTLE
2 NDC:52083-625-16 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2014-05-25


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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