WALMART DAYTIME AND NIGHTTIME MS SEVERE RELIEF VALUE PACK
WALMART DAYTIME AND NIGHTTIME MS SEVERE RELIEF VALUE PACK is an FDA drug label for the active ingredient ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCL manufactured by WAL-MART STORES INC. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260831.
- Generic name
- ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCL
- Manufacturer
- WAL-MART STORES INC
- Product type
- HUMAN OTC DRUG
- Route
- N/A
- Dosage form
- N/A
- NDC
- 79903-350
- Application
- M012
- Label effective
- 20260831
About this product
WALMART DAYTIME AND NIGHTTIME MS SEVERE RELIEF VALUE PACK is an FDA-registered drug product whose active ingredient is ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCL. It is labelled by WAL-MART STORES INC and marketed as a human otc drug product. Identifiers on file: NDC 79903-350, application M012, label effective 20260831. It is one of 2 FDA drug label records sharing the active ingredient ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCL. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCL are most often described in connection with: daytime severe, cold relief, temporarily relieves, symptoms due, minor aches, sore throat, pain headache, bronchial irritation. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses - Daytime Severe Cold Relief ▪ temporarily relieves these symptoms due to a cold: ▪ minor aches and pains ▪ minor sore throat pain ▪ headache ▪ cough due to minor throat and bronchial irritation ▪ temporarily reduces fever
Dosage & Administration
Directions – Daytime Severe Cold Relief ▪ do not use more than directed ▪ take every 4 hours, while symptoms persist. Do not take more than 6 packets in 24 hours unless directed by a doctor Age Dose Adults and children 12 years of age and over One packet Children under 12 years of age Do not use ▪ dissolve contents of one packet into 8 oz. hot water: sip while hot. Consume entire drink within 10 - 15 minutes. ▪ if using a microwave, add contents of one packet to 8 oz. of cool water: stir briskly before and after heating, Do not overheat Directions Nighttime Severe Cold Relief ▪ do not use more than directed ▪ take every 4 hours while symptoms persist, Do not take more than 5 packets in 24 hours unless directed by a doctor Age Dose Adults and Children 12 years of age and over One packet Children under 12 years of age do not use ▪ dissolve contents of one packet into 8 oz. hot water: sip while hot. Consume entire drink within 10 - 15 minutes. ▪ if using a microwave, add contents of one packet to 8 oz. of cool water: stir briskly before and after heating, Do not overheat.
Warnings
Warnings – Daytime Severe Cold Relief /Nighttime Severe Cold Relief Liver warning : This product contains acetaminophen. Severe liver damage may occur if you take ▪ more than 4,000 mg of acetaminophen in 24 hours ▪ with other drugs containing acetaminophen ▪ 3 or more alcoholic drinks every day while using this product Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include: ▪ skin reddening ▪ blisters ▪ rash If a skin reaction occurs, stop use and seek medical help right away Sore throat warning : If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.
More products with the same ingredient
ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCLHow products containing ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCL compare
FDA lists 2 drug label records with ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCL as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Genexa Inc. | 1 |
| — | — | WAL-MART STORES INC | 1 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is WALMART DAYTIME AND NIGHTTIME MS SEVERE RELIEF VALUE PACK used for?
Uses - Daytime Severe Cold Relief ▪ temporarily relieves these symptoms due to a cold: ▪ minor aches and pains ▪ minor sore throat pain ▪ headache ▪ cough due to minor throat and bronchial irritation ▪ temporarily reduces fever
Who makes WALMART DAYTIME AND NIGHTTIME MS SEVERE RELIEF VALUE PACK?
WAL-MART STORES INC is the labeler of record for WALMART DAYTIME AND NIGHTTIME MS SEVERE RELIEF VALUE PACK. 2 FDA label records share the active ingredient ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCL, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
Is WALMART DAYTIME AND NIGHTTIME MS SEVERE RELIEF VALUE PACK prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Are there other products containing ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCL?
Yes. 2 FDA drug label records list ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCL as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has WALMART DAYTIME AND NIGHTTIME MS SEVERE RELIEF VALUE PACK been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.