DM MAX CONGESTION AND COUGH- dextromethorphan hbr, guaifenesin solution

Drug Labeling and Warnings

Drug Details [pdf]

Drug Facts

Active ingredients
(in each 20 mL)
Dextromethorphan HBr 20 mg.
Guaifenesin 400 mg

Purpose

Dextromethorphan HBr .......Cough Suppressant
Guaifenesin .......................Expectorant

INDICATIONS & USAGE

Uses

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

WARNINGS

Warnings
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 DOCTOR

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

When using this product   do not use more than directed

WHEN USING

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

PREGNANCY OR BREAST FEEDING

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.

KEEP OUT OF REACH OF CHILDREN

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.

DOSAGE & ADMINISTRATION

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

OTHER SAFETY INFORMATION

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

INACTIVE INGREDIENT

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

QUESTIONS

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

DM Max Mucus Relief - Product Label

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"MORE FOR YOUR DOLLAR"

MARKET BASKET®

COMPARE TO Mucinex FAST-MAX™

DM MAX active ingredients*

Maximum Strength

DM Max

Mucus

Relief

CONGESTION & COUGH

Dextromethorphan HBr
Guaifenesin

COUGH SUPPRESSANT /
EXPECTORANT

ADULTS

 For Ages

12 and Over

6 FL OZ (177 mL)

DO NOT USE IF PRINTED NECKBAND IS BROKEN OR MISSING

DISTRIBUTED BY
DEMOULAS SUPERMARKETS INC.
875 East Street
Tewksbury, MA 01876

*This product is not manufactured or

distributed by Reckitt Benckiser Inc.,

distributor of Mucinex® FAST-MAX™

DM MAX.

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INGREDIENTS AND APPEARANCE

DM MAX  CONGESTION AND COUGH
dextromethorphan hbr, guaifenesin solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53942-518
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)
SODIUM SACCHARIN (UNII: SB8ZUX40TY)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SUCRALOSE (UNII: 96K6UQ3ZD4)
XANTHAN GUM (UNII: TTV12P4NEE)

Product Characteristics
Color	red	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53942-518-25	177 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	01/01/2026

Labeler - DeMoulas Market Basket (007869647)

Registrant - AptaPharma Inc. (790523323)

Establishment
Name	Address	ID/FEI	Business Operations
AptaPharma Inc.		790523323	manufacture(53942-518)