Sunmark Tussin (Guaifenesin) Solution [Mckesson] -

SUNMARK TUSSIN (GUAIFENESIN) SOLUTION [MCKESSON]
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NDC	49348-135-34, 49348-135-37
Set ID	a1e90b56-8b63-44b4-91f2-375f4bae0989
Category	HUMAN OTC DRUG LABEL
Packager	Strategic Sourcing Services LLC
Generic Name
Product Class
Product Number
Application Number	PART341

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Active ingredient (in each 10 mL)

Guaifenesin, USP 200 mg
Purpose

Expectorant
Use

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 is accompanied by 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

•

measure only with dosing cup provided

•

keep dosing cup with product

•

mL = milliliter

•

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 – 20 mL every 4 hours

children under 12 years

do not use
Other information

•

store at 20-25°C (68-77°F). Do not refrigerate.
Inactive ingredients

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

1-800-719-9260
Principal Display Panel

Adult tussin

Guaifenesin (Expectorant)

Mucus + Chest Congestion

200 mg

Relieves:

Mucus

Chest congestion

For ages 12 & over

Alcohol-free

NON-DROWSY

GLUTEN FREE

4 FL OZ (118 mL)

INGREDIENTS AND APPEARANCE

SUNMARK TUSSIN
guaifenesin solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49348-135
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	200 mg in 10 mL

Ingredient Name	Strength
Inactive Ingredients
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
CARAMEL (UNII: T9D99G2B1R)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GLYCERIN (UNII: PDC6A3C0OX)
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SODIUM BENZOATE (UNII: OJ245FE5EU)
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)

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

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:49348-135-34	1 in 1 CARTON	09/17/2014
1		118 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC:49348-135-37	1 in 1 CARTON	09/17/2014
2		236 mL in 1 BOTTLE; Type 0: Not a Combination Product