Label: MAXIMUM STRENGTH DM MAX- dextromethorphan hydrobromide, guaifenesin liquid
- NDC Code(s): 37808-518-25
- Packager: H E B
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 29, 2023
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
-
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
- WHEN USING
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
-
Product Label
Compare to Mucinex® FAST-MAX™
DM MAX active ingredients*
NDC 37808-518-25
H-E-B®
Maximum Strength
DM MAXDextromethorphan HBr /
Cough Suppressant
Guaifenesin / ExpectorantCongestion & Cough
Controls Cough
Thins & Loosens Mucus
Relieves Chest CongestionAdults
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
promiseIf 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-02112194-1905
0 41220 83197 5
Lot:
Exp:*This product is not manufactured or
distributed by Reekitt Benckiser Inc.,
distributor of Mucinex® FAST-MAXTM
DM MAXMADE WITH PRIDE & CARE FOR H-E-B®
SAN ANTONIO, TEXAS, 782044
res
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INGREDIENTS AND APPEARANCE
MAXIMUM STRENGTH DM MAX
dextromethorphan hydrobromide, guaifenesin liquidProduct 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 Drug M012 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)