NDC 53209-1003 – TYLENOL Cold Plus Flu Severe
Acetaminophen 325 mg/1; Dextromethorphan Hydrobromide 10 mg/1; Guaifenesin 200 mg/1; Phenylephrine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC53209-1003
Product details
- Brand name
- TYLENOL Cold Plus Flu Severe
- Generic name
- Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride
- Labeler
- Morning Star OTC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M012
- Marketed since
- June 19, 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/1
- Dextromethorphan Hydrobromide 10 mg/1
- Guaifenesin 200 mg/1
- Phenylephrine Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for TYLENOL Cold Plus Flu →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 53209-1003-2 | 25 BLISTER PACK in 1 POUCH (53209-1003-2) / 2 TABLET, FILM COATED in 1 BLISTER PACK (53209-1003-1) | Jun 19, 2025 |
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