Home NDC 0280-0084 Alka-Seltzer Hangover Relief
Product NDC 0280-0084
11-digit product format 002800084
Labeler code 0280
Product ID 0280-0084_414c4b16-847c-79f9-e063-6394a90a40bd
Type HUMAN OTC DRUG
Nonproprietary name ANHYDROUS CITRIC ACID, ASPIRIN, and SODIUM BICARBONATE
Dosage form TABLET, EFFERVESCENT
Route ORAL
Labeler Bayer HealthCare LLC.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-02-21
Substance CAFFEINE; ASPIRIN
Active strength 65; 500 mg/1; mg/1
Pharmacologic classes Anti-Inflammatory Agents, Non-Steroidal [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Methylxanthine [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], Xanthines [CS]
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 Hangover Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAFFEINE 65 mg/1 ASPIRIN 500 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3G6A5W338E Internal UNII lookup R16CO5Y76E Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1536815 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 0280-0084-01 Alka-Seltzer Hangover Relief 10 in 1 CARTON TABLET, EFFERVESCENT 10 16 0280-0084-01 Alka-Seltzer Hangover Relief 2 in 1 POUCH TABLET, EFFERVESCENT 2 16 0280-0084-02 Alka-Seltzer Hangover Relief 18 in 1 CARTON TABLET, EFFERVESCENT 18 16 0280-0084-02 Alka-Seltzer Hangover Relief 2 in 1 POUCH TABLET, EFFERVESCENT 2 16 0280-0084-03 Alka-Seltzer Hangover Relief 60 in 1 CARTON TABLET, EFFERVESCENT 60 16 0280-0084-03 Alka-Seltzer Hangover Relief 2 in 1 POUCH TABLET, EFFERVESCENT 2 16 0280-0084-04 Alka-Seltzer Hangover Relief 2 in 1 CARTON TABLET, EFFERVESCENT 2 16 0280-0084-04 Alka-Seltzer Hangover Relief 2 in 1 POUCH TABLET, EFFERVESCENT 2 16 0280-0084-05 Alka-Seltzer Hangover Relief 2 in 1 POUCH TABLET, EFFERVESCENT 2 16 0280-0084-05 Alka-Seltzer Hangover Relief 1600 in 1 BOX TABLET, EFFERVESCENT 1600 16 0280-0084-06 Alka-Seltzer Hangover Relief 30 in 1 CARTON TABLET, EFFERVESCENT 30 16 0280-0084-06 Alka-Seltzer Hangover Relief 2 in 1 POUCH TABLET, EFFERVESCENT 2 16
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0280-0084 ALKA-SELTZER HANGOVER RELIEF (ANHYDROUS CITRIC ACID, ASPIRIN, AND SODIUM BICARBONATE) TABLET, EFFERVESCENT [BAYER HEALTHCARE LLC.] 13 Current NDC, Legacy NDC, 12 package rows 20241210_dc235b06-999e-221d-e053-2a95a90a0ce1.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 4 of 79 · 1,579 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Gencare-Aspirin Low Dose Pain reliever (NSAID) ASPIRIN Pioneer Life Sciences, LLC 24d4f46a-c7a5-4e94-804f-1e307d8e8cfc 2026-08-09 Warnings Exact identifier application number: M013 Aspirin 81 mg ASPIRIN DOLGENCORP, LLC b4064039-2345-4227-b83d-54dc13a838d3 2026-08-07 Warnings Exact identifier application number: M013 Aspirin Low Dose ASPIRIN United Natural Foods, Inc. dba UNFI 87def9e0-0246-42cf-b8ea-2513d52e9f68 2026-08-07 Warnings Exact identifier application number: M013 berkley and jensen acetaminophen ACETAMINOPHEN BJWC dee57d73-73ac-48bb-b1da-9971f1ff21c4 2026-08-07 Warnings Exact identifier application number: M013 Pain Reliever PM Extra Strength ACETAMINOPHEN, DIPHENHYDRAMINE HCL Salado Sales, Inc. aef30709-f33d-48ff-b2d4-0639ffbd1ffd 2026-08-07 Warnings Exact identifier application number: M013 Aspirin ASPIRIN P & L Development, LLC 4cd74cec-a209-4e92-b853-fbe5c95f7678 2026-08-06 Warnings Exact identifier application number: M013 Tension Headache Aspirin-Free ACETAMINOPHEN, CAFFEINE Rite Aid Corporation 093a7c26-f2b1-4416-b193-81133d247d2e 2026-08-06 Warnings Exact identifier application number: M013 ACETAMINOPHEN ACETAMINOPHEN Kroger Company bc17b2e5-4828-6a2e-e053-2995a90a8c63 2026-08-05 Warnings Exact identifier application number: M013 Infants TYLENOL ACETAMINOPHEN Kenvue Brands LLC 997b9551-c222-4a9c-8ba1-09a5f97495fa 2026-08-05 Warnings Exact identifier application number: M013 Mantra Pain Gel raspberry ACETAMINOPHEN MOREMED INC. 7c8bdf49-a6d2-4e42-b006-375f103fd0ac 2026-08-05 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN HARRIS TEETER d2d2846d-4e0b-4d42-b300-60dd3b2cca1b 2026-08-05 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN HARRIS TEETER 960f5676-d8c5-470b-a663-4b8d152339b4 2026-08-05 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN HARRIS TEETER a60f6439-2033-4bd2-b78c-6c083414a12b 2026-08-05 Warnings Exact identifier application number: M013 pain relief PM ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE HARRIS TEETER 0afb6181-d0b1-4845-8230-faabf1b997dc 2026-08-05 Warnings Exact identifier application number: M013 Acetaminophen PM ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE Harris Teeter 8a3e3439-90ae-4fc9-8ff2-44b8363fa338 2026-08-05 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN Harris Teeter 50e7b939-e0eb-44ea-82ea-034e844e2c29 2026-08-05 Warnings Exact identifier application number: M013 pain relief aspirin Low Dose ASPIRIN Rite Aid Corporation df7835c9-f10f-40c6-8955-61423d94b677 2026-08-05 Warnings Exact identifier application number: M013 Aspirin Low Dose ASPIRIN DOLGENCORP, LLC 7396c97e-8a51-4a21-8208-f13258b5285c 2026-08-05 Warnings Exact identifier application number: M013 Pain Relief Regular Strength ACETAMINOPHEN Rite Aid Corporation 3b5d4a5a-8c65-4db1-bf01-e8df6523f45a 2026-08-04 Warnings Exact identifier application number: M013 childrens acetaminophen ACETAMINOPHEN WinCo Foods, LLC 4749a843-9c93-4edd-9b5f-a1e32666544e 2026-08-04 Warnings Exact identifier application number: M013
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 0280-0084-01 00280008401 10 POUCH in 1 CARTON (0280-0084-01) / 2 TABLET, EFFERVESCENT in 1 POUCH 10 pouch 2022-02-21 0000-00-00 No No Current 0280-0084-02 00280008402 18 POUCH in 1 CARTON (0280-0084-02) / 2 TABLET, EFFERVESCENT in 1 POUCH 18 pouch 2023-04-19 No No Current 0280-0084-03 00280008403 60 POUCH in 1 CARTON (0280-0084-03) / 2 TABLET, EFFERVESCENT in 1 POUCH 60 pouch 2023-04-19 No No Current 0280-0084-04 00280008404 2 POUCH in 1 CARTON (0280-0084-04) / 2 TABLET, EFFERVESCENT in 1 POUCH 2 pouch 2023-04-19 No No Current 0280-0084-05 00280008405 1600 POUCH in 1 BOX (0280-0084-05) / 2 TABLET, EFFERVESCENT in 1 POUCH 1600 pouch 2023-05-23 No No Current 0280-0084-06 00280008406 30 POUCH in 1 CARTON (0280-0084-06) / 2 TABLET, EFFERVESCENT in 1 POUCH 30 pouch 2025-10-13 No No Current