MAXIUM STRENGTH DM MAX- dextromethorphan hydrobromide, guaifenesin liquid

MAXIUM STRENGTH DM MAX by

Drug Labeling and Warnings

MAXIUM STRENGTH DM MAX by is a Otc medication manufactured, distributed, or labeled by Discount Drug Mart. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug FactsActive ingredients(in each 20 mL)

Dextromethorphan HBr, USP 20 mg

Guaifenesin 400 mg

Purpose

Cough Suppressant

Expectorant

Keep out of reach of children.

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

Uses

• helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes
• temporaroly relieves these symptoms occuring with a cold:
• cough due to minor throat and bronchial irritation

Warning

DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING.

Do not use

• for children under 12 years of age
• 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 lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema
• cough that occurs with too much phlegm (mucus)

When using this product

• do not use more than directed

Stop use and ask a doctor if

• cough lasts for more than 7 days, comes back, or occurs with fever, rash or persistant headache. These could be signs of a serious condition.

If pregnany or breast feeding,

ask a health professional before use.

Directions

• take only as recommended
• use dosage cup
• mL= millilter
• do not take more than 6 doses in any 24-hour period

• Age: Dose
• Adults & children 12 years adn older: 20 mL every 4 hours
• Children under 12 years of age: Do not use

Other information

• each 20 mL contains: sodium 12 mg
• dosage cup provided
• store between 15-30°C (59-86°F)
• do not refrigerate

Inactive ingredients

anhydrous citric acid, dextrose, D&C Red # 33, FD&C Red # 40, flavors, glycerin, maltitol, propylene glycol, purified water, saccharin sodium, sodium benzoate, sucralose, Xanthan gum

Questions?

Call weekdays from 9:30 AM to 4:30 PM EST at 1-877-798-5944

DISCOUNT drug mart FOOD FAIR MAXIUM STRENGTH DM MAX product label

*COMPARE TO THE ACTIVE INGREDIENTS IN MUCINEX® FAST-MAX™-DM MAX

LF-010

DISCOUNT

drug mart

FOOD FAIR

MAXIUM STRENGTH DM MAX

Dextromethorphan HBr/ Guaifenesin

COUGH SUPPRESSANT/

EXPECTORANT

Controls Cough

Thins & Loosens mucus

Relieves Chest Congestion

Adults

For Ages 12 & Over

6 FL OZ (177 mL)

* This product is not manufactured or distributed by Reckitt Benckiser Inc., distributor of MUCINEX® FAST-MAX™ DM MAX

LB - 010 LOT: EXP:

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SATISFACTION GUARANTEED
IF DISSASIFIED , RETURN UNUSED PORTION AND PACKAGE TO STORE WHERE PURCHASED. IF UNABLE TO RETURN TO STORE, SEND REASON FOR DISSATISFACTION, NAME, ADDRESS AND EMPTY PACKAGE TO: DISCOUNT DRUG MART, 211 COMMERCE DRIVE, MEDINA, OHIO 44256

INGREDIENTS AND APPEARANCE

MAXIUM STRENGTH DM MAX 
dextromethorphan hydrobromide, guaifenesin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53943-518
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	20 mg  in 20 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	400 mg  in 20 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
DEXTROSE (UNII: IY9XDZ35W2)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GLYCERIN (UNII: PDC6A3C0OX)
MALTITOL (UNII: D65DG142WK)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SUCRALOSE (UNII: 96K6UQ3ZD4)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53943-518-25	117 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/10/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	12/10/2013

Labeler - Discount Drug Mart (047741335)