NDC 11673-410 – Mucus Relief Severe Cold Daytime Maximum Strength
Dextromethorphan Hydrobromide 20 mg/20mL; Acetaminophen 650 mg/20mL; Guaifenesin 400 mg/20mL; Phenylephrine Hydrochloride 10 mg/20mL · Liquid · Oral
Product NDC11673-410
Product details
- Brand name
- Mucus Relief Severe Cold Daytime Maximum Strength
- Generic name
- Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl
- Labeler
- TARGET Corporation
- Dosage form
- Liquid
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M012
- Marketed since
- August 31, 2016
- Marketing end
- December 31, 2026
- Pharmacologic class
- Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist; alpha-1 Adrenergic Agonist
Active ingredients
- Dextromethorphan Hydrobromide 20 mg/20mL
- Acetaminophen 650 mg/20mL
- Guaifenesin 400 mg/20mL
- Phenylephrine Hydrochloride 10 mg/20mL
Uses, dosage, side effects and warnings for Mucus Relief Severe Cold →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 11673-410-06 | 177 mL in 1 BOTTLE, PLASTIC (11673-410-06) | Aug 31, 2016 |