Home NDC 0280-1630 Alka-Seltzer Plus Maximum Strength Day Cold and Flu PowerMax Gels
Product NDC 0280-1630
11-digit product format 002801630
Labeler code 0280
Product ID 0280-1630_45267e98-74cd-6121-e063-6294a90a5166
Type HUMAN OTC DRUG
Nonproprietary name acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride
Dosage form CAPSULE, LIQUID FILLED
Route ORAL
Labeler Bayer HealthCare LLC.
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-07-02
Substance DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; ACETAMINOPHEN
Active strength 10; 5; 325 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 2026-12-31
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 Alka-Seltzer Plus Maximum Strength Day Cold and Flu PowerMax Gels
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DEXTROMETHORPHAN HYDROBROMIDE 10 mg/1 PHENYLEPHRINE HYDROCHLORIDE 5 mg/1 ACETAMINOPHEN 325 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 9D2RTI9KYH Internal UNII lookup 04JA59TNSJ Internal UNII lookup 362O9ITL9D 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.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0280-1630-16 Alka-Seltzer Plus Maximum Strength Day Cold and Flu PowerMax Gels 8 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 8 7 0280-1630-16 Alka-Seltzer Plus Maximum Strength Day Cold and Flu PowerMax Gels 2 in 1 CARTON CAPSULE, LIQUID FILLED 2 7 0280-1630-24 Alka-Seltzer Plus Maximum Strength Day Cold and Flu PowerMax Gels 8 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 8 7 0280-1630-24 Alka-Seltzer Plus Maximum Strength Day Cold and Flu PowerMax Gels 3 in 1 CARTON CAPSULE, LIQUID FILLED 3 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0280-1630 ALKA-SELTZER PLUS MAXIMUM STRENGTH DAY COLD AND FLU POWERMAX GELS (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE) CAPSULE, LIQUID FILLED [BAYER HEALTHCARE LLC.] 6 Current NDC, Legacy NDC, 4 package rows 20240821_6f2d18f6-935f-9215-e053-2a91aa0aedd3.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 0280-1630-16 00280163016 2 BLISTER PACK in 1 CARTON (0280-1630-16) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 2 blister pack 2018-07-02 0000-00-00 No No Current 0280-1630-24 00280163024 3 BLISTER PACK in 1 CARTON (0280-1630-24) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 3 blister pack 2018-07-02 0000-00-00 No No Current