Home NDC 85237-1956 TYLENOL Cold Plus Flu
Product NDC 85237-1956
11-digit product format 852371956
Labeler code 85237
Product ID 85237-1956_55bdcb18-a65a-d916-e063-6294a90a7f17
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Select Consumer Group
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-09-01
Substance ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Active strength 325; 10; 200; 5 mg/1; mg/1; mg/1; mg/1
Pharmacologic classes Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base TYLENOL Cold Plus Flu
Brand name suffix Severe
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 325 mg/1 DEXTROMETHORPHAN HYDROBROMIDE 10 mg/1 GUAIFENESIN 200 mg/1 PHENYLEPHRINE HYDROCHLORIDE 5 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1110988 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# 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.
Matched openFDA labels page 74 of 180 · 3,583 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85237-1956-1 85237195601 1 POUCH in 1 BLISTER PACK (85237-1956-1) / 2 TABLET, FILM COATED in 1 POUCH (85237-1956-0) 1 pouch 2024-09-11 No No Current 85237-1956-2 85237195602 2 POUCH in 1 BLISTER PACK (85237-1956-2) / 2 TABLET, FILM COATED in 1 POUCH (85237-1956-0) 2 pouch 2024-09-11 No No Current 85237-1956-3 85237195603 20 POUCH in 1 BOX (85237-1956-3) / 2 TABLET, FILM COATED in 1 POUCH (85237-1956-0) 20 pouch 2024-09-11 No No Current 85237-1956-4 85237195604 25 POUCH in 1 BOX (85237-1956-4) / 2 TABLET, FILM COATED in 1 POUCH (85237-1956-0) 25 pouch 2024-09-11 No No Current 85237-1956-6 85237195606 50 POUCH in 1 BOX (85237-1956-6) / 2 TABLET, FILM COATED in 1 POUCH (85237-1956-0) 50 pouch 2024-09-11 No No Current 85237-1956-7 85237195607 3 POUCH in 1 BLISTER PACK (85237-1956-7) / 2 TABLET, FILM COATED in 1 POUCH (85237-1956-0) 3 pouch 2024-09-11 No No Current