MAXIMUM STRENGTH DM MAX- dextromethorphan hydrobromide, guaifenesin liquid

Maximum Strength DM MAX by

Drug Labeling and Warnings

Maximum Strength DM MAX by is a Otc medication manufactured, distributed, or labeled by H E B, AptaPharma Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

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
symploms 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 oxiclase
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

STOP USE

Slop 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

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

  Age                        Dose

Adults &                   20 ml
children 12               every 4
years and                 hours
older

Children               Do not use
under 12
Years of age

OTHER SAFETY INFORMATION

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

INACTIVE INGREDIENT

Inactive ingredients
anhydrous citric acid,
dextrose, D&C Red #33, FD&C
Red #40, flavors, glycerin,
maltitol, propylene glycol,
purified waler, 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

Product Label

Compare to Mucinex® FAST-MAX™

DM MAX active ingredients*

NDC: 37808-518-25

H-E-B®

Maximum Strength
DM MAX

Dextromethorphan HBr /
Cough Suppressant
Guaifenesin  / Expectorant

Congestion & Cough

Controls Cough
Thins & Loosens Mucus
Relieves Chest Congestion

Adults

For Ages 12 & Over

6 FL OZ (177mL)

LF 021

Peel Corner to Read Complete
Drug Facts and Information →

DO NOT USE IF PRINTED SEAL

UNDER CAP IS TORN OR MISSING

             H-E-B®

100%
GUARANTEE
promise

If you aren't completely pleased
with this product, we'll be happy to
replace it or refund your money.
You have our word on it.

LB-021

12194-1905

0 41220 83197 5

Lot:
Exp:

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

MADE WITH PRIDE & CARE FOR H-E-B®

SAN ANTONIO, TEXAS, 782044

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INGREDIENTS AND APPEARANCE

MAXIMUM STRENGTH DM MAX 
dextromethorphan hydrobromide, guaifenesin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37808-518
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: 37808-518-25	177 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/14/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	09/14/2012

Labeler - H E B (007924756)

Registrant - AptaPharma Inc. (790523323)

Establishment
Name	Address	ID/FEI	Business Operations
AptaPharma Inc.		790523323	manufacture(37808-518)