• 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: • runny nose • sneezing • itchy, watery eyes • itching of the nose or throat • controls the impulse to cough to help you sleep
• measure only with dosing cup provided • keep dosing cup with product • mL = milliliter • do not take more than 4 doses in any 24-hour period • this adult product is not intended for use in children under 12 years of age age dose adults and children 12 years and over 20 mL every 6 hours children under 12 years do not use
• each 20 mL contains: sodium 11 mg • store at 20-25°C (68-77°F)
Dextromethorphan HBr, USP 30 mg
Doxylamine succinate, USP 12.5 mg
Cough suppressant
Antihistamine
taking sedatives or tranquilizers
cough lasts for more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
age | dose |
adults and children 12 years and over | 20 mL every 6 hours |
children under 12 years | do not use |
anhydrous citric acid, benzoic acid, benzyl alcohol, carboxymethylcellulose sodium, FD&C blue #1, FD&C red #40, flavor, glycerin, menthol, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sorbitol solution, sucralose, xanthan gum
1-800-719-9260
Dextromethorphan HBr, USP 20 mg
Guaifenesin, USP 400 mg
Cough suppressant
Expectorant
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.
cough lasts for more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
age | dose |
adults and children 12 years and over | 20 mL every 4 hours |
children under 12 years | do not use |
acetic acid, anhydrous citric acid, carboxymethylcellulose sodium, FD&C blue no. 1, FD&C red no. 40, flavor, glycerin, menthol, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol solution, sucralose, xanthan gum
1-800-719-9260
DAY & NIGHT PACK
Compare to Robitussin® Maximum Strength Cough + Chest Congestion DM & Robitussin® Maximum Strength Nighttime Cough DM active ingredients
ADULT
NON-DROWSY
Wal-Tussin®
DM Max
COUGH & CHEST CONGESTION DM
DEXTROMETHORPHAN HBr / COUGH SUPPRESSANT
GUAIFENESIN / EXPECTORANT
MAXIMUM STRENGTH
ALCOHOL FREE
Relieves cough, chest congestion & mucus
For maximum strength mucus relief
12 years & older
SEE NEW DOSING
RASPBERRY MENTHOL FLAVOR
ADULT
Nighttime Wal-Tussin® DM Max
COUGH
DEXTROMETHORPHAN HBr / COUGH SUPPRESSANT
DOXYLAMINE SUCCINATE / ANTIHISTAMINE
MAXIMUM STRENGTH
ALCOHOL FREE
Relieves cough, itchy throat & runny nose
12 years & older
SEE NEW DOSING
RASPBERRY, BLACKBERRY & MENTHOL FLAVOR
TOTAL 8 FL OZ (236 mL) – 2 x 4 FL OZ (118 mL)
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0363-0913-12 | ML - Milliliter | 0363-0913 | 8b2c8232-c6d6-48fa-99ed-b2f12b45617f | 1 | 2022-06-06 |
| 0363-1023-26 | ML - Milliliter | 0363-1023 | fb849a90-e2c9-481a-ae3e-986c6463f395 | 1 | 2022-06-06 |
| 0363-1023-34 | ML - Milliliter | 0363-1023 | 8f2f9698-2c5d-47ef-81a0-dfdd6b5f9174 | 1 | 2022-06-06 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 0363-0913 | 0363-0913-12 |
| 0363-1023 | 0363-1023-26 |
Every source-derived ingredient row is available through these pages.
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| fee5b5d6-e679-4da4-ad87-63accfa9a9aa | d7a00a92-7d41-4a6e-b84c-9e20514cbc4a | 2024-11-11 | Warnings | d7a00a92-7d41-4a6e-b84c-9e20514cbc4a |
Adverse event summaries are temporarily unavailable. Other product information remains available.