ADULT TUSSIN DM LIL DRUG STORE PRODUCTS- dextromethorphan hydrobromide and guaifenesin liquid

Adult Tussin DM by

Drug Labeling and Warnings

Adult Tussin DM by is a Otc medication manufactured, distributed, or labeled by Lil' Drug Store Products, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredients (in each 10 mL)	Purposes
Dextromethorphan HBr 20 mg	Cough suppressant
Guaifenesin 200 mg	Expectorant

Uses

• temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
• helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes

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

• 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 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 (1-800-222-1222) right away.

Directions

• do not take more than 6 doses in any 24-hour period
• measure only with dosing cup provided. Do not use any other dosing device.
• keep dosing cup with product
• mL = milliliter
• this adult product is not intended for use in children under 12 years of age
• adults and children 12 years and over: 10 mL every 4 hours
• children under 12 years: do not use

Other information

• store between 68-77° F (20-25° C). Do not refrigerate.

Inactive ingredients

citric acid, FD&C red #40, flavor, glucose, glycerin, high fructose corn syrup, menthol, purified water, saccharin sodium, sodium benzoate

Questions or comments?

Call toll-free 1-877-507-6516 (M-F 8AM-4:30PM CST)

SPL UNCLASSIFIED SECTION

Distributed by:
Lil' Drug Store Products, Inc.
1201 Continental Place NE
Cedar Rapids, IA 52402

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Carton

QUALITY
GUARANTEED

Compare to the Active Ingredients
in Robitussin® Peak Cold
Cough + Chest Congestion DM*

Adult
Tussin DM

Dextromethorphan HBr 20 mg, Guaifenesin 200 mg
Cough Suppressant, Expectorant

Non-Drowsy Relief of

• Cough
• Chest Congestion / Mucus

For ages 12 years and over

4 FL OZ
(118 mL)

Lil'
Drug Store®

INGREDIENTS AND APPEARANCE

ADULT TUSSIN DM   LIL DRUG STORE PRODUCTS
dextromethorphan hydrobromide and guaifenesin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66715-6858(NDC:49580-0385)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (Dextromethorphan - UNII:7355X3ROTS)	Dextromethorphan Hydrobromide	10 mg  in 5 mL
Guaifenesin (UNII: 495W7451VQ) (Guaifenesin - UNII:495W7451VQ)	Guaifenesin	100 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
Citric Acid Monohydrate (UNII: 2968PHW8QP)
FD&C Red No. 40 (UNII: WZB9127XOA)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
Glycerin (UNII: PDC6A3C0OX)
High Fructose Corn Syrup (UNII: XY6UN3QB6S)
Menthol, Unspecified Form (UNII: L7T10EIP3A)
Water (UNII: 059QF0KO0R)
Saccharin Sodium (UNII: SB8ZUX40TY)
Sodium benzoate (UNII: OJ245FE5EU)

Product Characteristics
Color	RED	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66715-6858-4	1 in 1 CARTON	09/09/2016
1		118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part341	12/01/2014

Labeler - Lil' Drug Store Products, Inc (093103646)