DM MAX MAXIUM STRENGTH- dextromethorphan hydrobromide, guaifenesin liquid

DM MAX by

Drug Labeling and Warnings

DM MAX by is a Otc medication manufactured, distributed, or labeled by Chain Drug Consortium, LLC, AptaPharma Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Drug Facts

Active ingredients (in each 20 mL)

Dextromethorphan HBr 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 to 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

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 two weeks after stopping the MAOI drug. If you do not know if your child’s prescription drug contains an MAOI, ask a doctor or a pharmacist before taking this product.

• for children under 12 years of age

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)
  

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.

When using this product

• do not use more than directed

If pregnant or breast feeding

ask a health professional before use.

Directions

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

Other information

    each 20 mL teaspoon contains:

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

Inactive ingredients

citric acid anhydrous, dextrose, D and C Red # 33,dextrose, FD and 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

Product Label

NDC: 68016-222-00

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

Premier Value®


Maxium Strength
DM MAX

Dextromethorphan HBr / Guaifenesin
COUGH SUPPRESSANT / EXPECTORANT

    * Controls Cough
    * Thins and Loosens Mucus
    * Relieves Chest Congestion

Adults

For Ages 12 and Over

 6 FL OZ (177mL)

INDEPENDENTLY TESTED SATISFACTION GUARANTEED PV
DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING

Peel Corner to read Complete Drug Facts and Information     

Lot:    Exp:

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

If for Any reason you are not satisfied with this product, lease return it to the store where purchased for a full refund.

DISTRIBUTED BY
CHAIN DRUG CONSORTIUM
3301 NW BOCA RATON BLVD
SUITE 101, BOCA RATON, FL 33431

LF-003

INGREDIENTS AND APPEARANCE

DM MAX  MAXIUM STRENGTH
dextromethorphan hydrobromide, guaifenesin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68016-222
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: 68016-222-00	177 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	01/01/2013

Labeler - Chain Drug Consortium, LLC (101668460)

Registrant - AptaPharma Inc. (790523323)

Establishment
Name	Address	ID/FEI	Business Operations
AptaPharma Inc.		790523323	manufacture(68016-222)