Robitussin Maximum Strength Nighttime Cough DM description, usages, side effects, indications, overdosage, supplying and lots more!

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Robitussin Maximum Strength Nighttime Cough DM

Richmond Division of Wyeth
Pfizer Inc

ROBITUSSIN MAXIMUM STRENGTH NIGHTTIME COUGH DM


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients (in each 10 ml) Purposes
Dextromethorphan HBr, USP 30 mg Cough suppressant
Doxylamine Succinate, USP 12.5 mg Antihistamine
  • temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
  • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
    • runny nose
    • sneezing
    • itchy, watery eyes
    • itching of the nose or throat
  • controls the impulse to cough to help you sleep

Do not use

  • to sedate a child or to 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 product.

Ask a doctor before use if you have

  • trouble urinating due to an enlarged prostate gland
  • glaucoma
  • a cough that occurs with too much phlegm (mucus)
  • a breathing problem or chronic cough that lasts or as occurs with smoking, asthma, chronic bronchitis or emphysema

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

When using this product

  • do not use more than directed
  • marked drowsiness may occur
  • avoid alcoholic drinks
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • be careful when driving a motor vehicle or operating machinery
  • excitability may occur, especially in children

Stop use and ask a doctor if cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

  • measure only with dosing cup provided
  • keep dosing cup with product
  • ml = milliliter
  • do not take more than 4 doses in any 24-hour period
  • this adult product is not intended for use in children under 12 years of age
age dose
adults and children 12 years and over 10 ml every 6 hours
children under 12 years do not use
  • each 10 ml contains: sodium 7 mg
  • store at 20-25°C (68-77°F)

anhydrous citric acid, FD&C Red No. 40, glycerin, high fructose corn syrup, menthol, natural flavor, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sodium citrate, sucralose, xanthan gum

call weekdays from 9 AM to 5 PM EST at 1-800-762-4675

For most recent product information,
visit www.robitussin.com

Distributed by:
Pfizer, Madison, NJ 07940 USA

PRINCIPAL DISPLAY PANEL - 237 mL Bottle Carton

ADULT

NEW!

Robitussin®

MAXIMUM
STRENGTH

Nighttime
Cough DM

DEXTROMETHORPHAN HBr (Cough Suppressant)
DOXYLAMINE SUCCINATE (Antihistamine)

Relieves:

  • Cough
  • Itchy Throat
  • Runny Nose

DM
NIGHTTIME
MAX

Max Strength
Nighttime
Cough Control

8 FL OZ
(237 ml)

For Ages 12 & Over

Robitussin Maximum Strength Nighttime Cough DM

Robitussin Maximum Strength Nighttime Cough DM

DEXTROMETHORPHAN HYDROBROMIDE and DOXYLAMINE SUCCINATE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0031-8717
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DEXTROMETHORPHAN HYDROBROMIDE DEXTROMETHORPHAN 30 mg
DOXYLAMINE SUCCINATE DOXYLAMINE 12.5 mg

Inactive Ingredients

Ingredient Name Strength
ANHYDROUS CITRIC ACID
FD&C RED NO. 40
GLYCERIN
HIGH FRUCTOSE CORN SYRUP
MENTHOL
POLYETHYLENE GLYCOLS
propylene glycol
water
SODIUM BENZOATE
SODIUM CITRATE
Sucralose
XANTHAN GUM

Product Characteristics

Color
RED

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 118 in 1 BOTTLE
2 237 in 1 BOTTLE
3 NDC:0031-8717-18 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2013-03-01


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Be sure to consult your doctor before taking any medication!
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