DM MAX- dextromethorphan hbr, guaifenesin, phenylephrine hcl solution

DM Max by

Drug Labeling and Warnings

DM Max by is a Otc medication manufactured, distributed, or labeled by Best Choice, AptaPharma Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Drug Facts

Active ingredients

(in each 20 mL)

Dextromethorphan HBr 20 mg
Guaifenesin 400 mg

PURPOSE

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 ocurring 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 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

STOP USE

Stop use and ask a doctor if

■ cough lasts for more than 7 days
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.

In case of overdose, gel medical help or contact a
Poison Control Genter rightaway.

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.

DOSAGE & ADMINISTRATION

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

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

OTHER SAFETY INFORMATION

Other information
■ 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 Blue #33, FD&C Red#40,

flavors, glycerin, maltitol,

propylene 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

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Product Label: Best Choice® DM Max

Best Choice®

MAXIMUM STRENGTH

DM Max

6 FL OZ (177 mL)

PROUDLY DISTRIBUTED BY:

VALUE MERCHANDISERS, CO.

5000 KANSAS AVE

KANSAS CITY, KS 66106

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 
dextromethorphan hbr, guaifenesin, phenylephrine hcl solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63941-518
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)

Product Characteristics
Color	red	Score
Shape		Size
Flavor	CHERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63941-518-25	177 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	01/01/2025

Labeler - Best Choice (868703513)

Registrant - AptaPharma Inc. (790523323)

Establishment
Name	Address	ID/FEI	Business Operations
AptaPharma Inc.		790523323	manufacture(63941-518)