HEALTH MART ADULT TUSSIN- guaifenesin syrup
McKesson

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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McKesson Adult Tussin Drug Facts

Active ingredient (in each 5 mL tsp)

Guaifenesin, USP 100 mg

Purpose

Expectorant

Uses

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

Warnings

Ask a doctor before use if you have

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

Stop use and ask a doctor if

cough lasts for more than 7 days, comes back, or occurs with fever, rash, or persistent headache. A persistent cough may be a sign 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. (1-800-222-1222)

Directions

•: do not take more than 6 doses in any 24-hour period
•: use only with enclosed measuring cup. Do not use any other device.
•: this adult product is not intended for use in children under 12 years of age

age	dose
adults and children 12 years and over	2-4 teaspoons (tsp) every 4 hours
children under 12 years	do not use

Other information

•: store at 20-25°C (68-77°F)

Inactive ingredients

anhydrous citric acid, caramel, FD&C red no. 40, flavor, glycerin, high fructose corn syrup, maltol, menthol, propylene glycol, purified water, saccharin sodium, sodium benzoate

Questions or comments?

1-800-719-9260

Principal Display Panel

compare to Adult Robitussin® Mucus + Chest Congestion active ingredient

for ages 12 & over

adult tussin

chest congestion

expectorant (guaifenesin, USP)

relieves chest congestion and mucus

non-drowsy

alcohol free

gluten free

cherry flavor

HEALTH MART ADULT TUSSIN
guaifenesin syrup

Product Information
Product Type	HUMAN OTC DRUG LABEL	Item Code (Source)	NDC:62011-0089
Route of Administration	ORAL	DEA Schedule

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
GUAIFENESIN (GUAIFENESIN)	GUAIFENESIN	100 mg in 5 mL

Ingredient Name	Strength
Inactive Ingredients
ANHYDROUS CITRIC ACID
CARAMEL
FD&C RED NO. 40
GLYCERIN
HIGH FRUCTOSE CORN SYRUP
PROPYLENE GLYCOL
WATER
SACCHARIN SODIUM
SODIUM BENZOATE
MALTOL
MENTHOL

Product Characteristics
Color	RED (dark)	Score
Shape		Size
Flavor	CHERRY	Imprint Code
Contains

#	Item Code	Package Description
Packaging
1	NDC:62011-0089-1	1 in 1 CARTON
1		237 mL in 1 BOTTLE
2	NDC:62011-0089-2	1 in 1 CARTON
2		118 mL in 1 BOTTLE

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part341	01/11/2012

Labeler - McKesson (177667227)

Revised: 8/2013

Document Id: 8b74a850-787f-4606-8a77-98ce684ec685

Set id: b3a23194-c571-486a-9d34-6ffeed98e165

Version: 2

Effective Time: 20130806

McKesson