NDC 59640-308 – Daytime Severe
Acetaminophen 325 mg/15mL; Dextromethorphan Hydrobromide 10 mg/15mL; Guaifenesin 200 mg/15mL; Phenylephrine Hydrochloride 5 mg/15mL · Solution · Oral
Product NDC59640-308
Product details
- Brand name
- Daytime Severe
- Generic name
- Acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride
- Labeler
- H E B
- Dosage form
- Solution
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M012
- Marketed since
- August 5, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist; alpha-1 Adrenergic Agonist
Active ingredients
- Acetaminophen 325 mg/15mL
- Dextromethorphan Hydrobromide 10 mg/15mL
- Guaifenesin 200 mg/15mL
- Phenylephrine Hydrochloride 5 mg/15mL
Uses, dosage, side effects and warnings for Daytime severe →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 59640-308-40 | 355 mL in 1 BOTTLE (59640-308-40) | Aug 5, 2025 |
Other Daytime severe products
- 51316-613 Acetaminophen 325 mg/15mL; Dextromethorphan Hydrobromide 10 mg/15mL;… · Solution · CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED