Home NDC 69842-897 Daytime Cold and Flu
Product NDC 69842-897
11-digit product format 698420897
Labeler code 69842
Product ID 69842-897_185d7b73-b8ce-4e68-b45c-417435c8b2d9
Type HUMAN OTC DRUG
Nonproprietary name ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCL
Dosage form CAPSULE, LIQUID FILLED
Route ORAL
Labeler CVS Pharmacy
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-07-31
Substance ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Active strength 325; 10; 5 mg/1; mg/1; mg/1
Pharmacologic classes Adrenergic alpha1-Agonists [MoA], 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 Daytime Cold and Flu
Brand name suffix Non Drowsy
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 325 mg/1 DEXTROMETHORPHAN HYDROBROMIDE 10 mg/1 PHENYLEPHRINE HYDROCHLORIDE 5 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup 9D2RTI9KYH Internal UNII lookup 04JA59TNSJ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1086997 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69842-897-16 Daytime Cold and FluNon Drowsy 1 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 1 7 69842-897-16 Daytime Cold and FluNon Drowsy 16 in 1 CARTON CAPSULE, LIQUID FILLED 16 7 69842-897-24 Daytime Cold and FluNon Drowsy 24 in 1 CARTON CAPSULE, LIQUID FILLED 24 7 69842-897-24 Daytime Cold and FluNon Drowsy 1 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 1 7 69842-897-48 Daytime Cold and FluNon Drowsy 48 in 1 CARTON CAPSULE, LIQUID FILLED 48 7 69842-897-48 Daytime Cold and FluNon Drowsy 1 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 1 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-897 DAYTIME COLD AND FLU NON DROWSY (ACETAMINOHPEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL) CAPSULE, LIQUID FILLED [CVS PHARMACY] 4 Current NDC, Legacy NDC, 6 package rows 20240308_c71427d4-707f-411f-8bd4-133517a9992b.zip
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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69842-897-16 69842089716 16 BLISTER PACK in 1 CARTON (69842-897-16) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 16 blister pack 2019-07-31 No No Current 69842-897-24 69842089724 24 BLISTER PACK in 1 CARTON (69842-897-24) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 24 blister pack 2019-07-31 0000-00-00 No No Current 69842-897-48 69842089748 48 BLISTER PACK in 1 CARTON (69842-897-48) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 48 blister pack 2019-07-31 0000-00-00 No No Current