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Tussin

Bio-Pharm, Inc.

Tussin


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient (in each 5mL TSP (teaspoon))

Guaifenesin USP 100 mg

Purpose

Expectorant

Tussin Uses

helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive

Warnings

Ask a doctor before use if you have

  • a cough that lasts or a chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema
  • a cough occurs with too much phlegm (mucus)

Stop use and ask a doctor: if cough lasts for more than 7 days, comes back, or occurs with fever, rash, or headache that lasts. These could be signs of a serious condition.

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

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

Directions

  • use only enclosed dosing cup to dose this product
  • do not take more than 6 doses in any 24 hour period
  • this product is not intended for use in children under 12 years of age
adults and children 12 years and over 2-4 TSP every 4 hours or as directed by doctor
children under 12 years do not use

Tussin Other information

  • each TSP (5 mL) contains: sodium 3 mg
  • TAMPER-EVIDENT: Do not use this product if inner foil seal over the mouth of the bottle is cut, torn, broken or missing
  • store at 20°-25°C (68°-77°F)

Inactive ingredients

caramel powder, citric acid, corn syrup, FD&C Red #40, glycerin, menthol, propylene glycol, purified water, sodium benzoate, sodium saccharin

Questions or comments?

866-845-1611

DISTRIBUTED BY
GREENBRIER INTERNATIONAL, INC.
500 VOLVO PARKWAY
CHESAPEAKE, VA 23320

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Carton

COMPARE TO ACTIVE INGREDIENT IN
ROBITUSSIN®*

NDC 59741-112-10

ASSURED

ADULT

Tussin

Guaifenesin Oral
Solution, USP

Expectorant

AGES 12+

  • Alcohol Free
  • Non-Drowsy

Relieves Chest
Congestion & Mucus

4 FL OZ
(118 mL)

Tussin

Tussin

Guaifenesin SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59741-112
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Guaifenesin GUAIFENESIN 100 mg

Inactive Ingredients

Ingredient Name Strength
propylene glycol
SODIUM BENZOATE
saccharin sodium
CITRIC ACID MONOHYDRATE
GLYCERIN
MENTHOL
water
CORN SYRUP
CARAMEL
FD&C RED NO. 40

Product Characteristics

Color
BROWN (Reddish-Brown)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 118 in 1 BOTTLE
2 NDC:59741-112-10 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2014-04-08


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