Label: TUSSIN DM MAX NIGHTTIME- dextromethorphan hbr, doxylamine succinate solution
- NDC Code(s): 49035-943-19
- Packager: Wal-Mart Stores Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated April 4, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients (in each 20 mL)
- Purpose
-
Uses
- temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
- temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
- itching of the nose or throat
- runny nose
- itchy, watery eyes
- sneezing
- controls the impulse to cough to help you sleep
-
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 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
- a cough that occurs with too much phlegm (mucus)
- difficulty in urination due to enlargement of the prostate gland
- glaucoma
- a breathing problem or persistent or chronic cough as occurs with smoking, asthma, chronic bronchitis, or emphysema
When using this product
- marked drowsiness may occur
- avoid alcoholic drinks
- alcohol, sedatives, and tranquilizers may increase drowsiness
- use caution when driving a motor vehicle or operating machinery
- excitability may occur, especially in children
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
equate™
NDC 49035-943-19
Compare to
Robitussin®
Maximum Strength
Nighttime
Cough DM Active
Ingredients†Maximum Strength
Nighttime
Tussin DM MaxDextromethorphan HBr -
Cough Suppressant
Doxylamine Succinate -
AntihistamineNighttime Cough DM
Relief of:
• Cough
• Itchy throat
• Runny noseAges 12 +
Oral Solution
Dosage cup included
8 FL OZ (237 mL)
TAMPER EVIDENT: DO NOT USE IF IMPRINTED
SAFETY SEAL UNDER CAP IS BROKEN OR MISSING
TAMPER EVIDENT: DO NOT USE IF
PRINTED NECK WRAP IS BROKEN
OR MISSINGPARENTS:
Learn about teen medicine abuse
www.StopMedicineAbuse.orgSatisfaction guaranteed – Or we’ll replace it or give
you your money back. For questions or comments
or to report an undesired reaction or side effect,
please call 1-888-287-1915.DISTRIBUTED BY: Walmart Inc.,
Bentonville, AR 72716†This product is not manufactured or distributed by Wyeth
LLC, owner of the registered trademark Robitussin®
Maximum Strength Nighttime Cough DM.
50844 REV0123A04319Equate 44-043
-
INGREDIENTS AND APPEARANCE
TUSSIN DM MAX NIGHTTIME
dextromethorphan hbr, doxylamine succinate solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-943 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 30 mg in 20 mL DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL) DOXYLAMINE SUCCINATE 12.5 mg in 20 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERIN (UNII: PDC6A3C0OX) HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CHLORIDE (UNII: 451W47IQ8X) TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K) SUCRALOSE (UNII: 96K6UQ3ZD4) SUCROSE (UNII: C151H8M554) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color red (Maroon) Score Shape Size Flavor MENTHOL, BERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-943-19 1 in 1 CARTON 08/15/2018 1 237 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 08/15/2018 Labeler - Wal-Mart Stores Inc (051957769) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 manufacture(49035-943) , pack(49035-943)