Home NDC 70264-029 MOTRIN IB
Product NDC 70264-029
11-digit product format 702640029
Labeler code 70264
Product ID 70264-029_43c8bb40-2da9-05a2-e063-6394a90ad6c5
Type HUMAN OTC DRUG
Nonproprietary name IBUPROFEN
Dosage form TABLET, FILM COATED
Route ORAL
Labeler R J General Corporation
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-05-01
Substance IBUPROFEN
Active strength 200 mg/1
Pharmacologic classes Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [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 MOTRIN IB
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength IBUPROFEN 200 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination WK2XYI10QM Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 201126 Internal RxNorm lookup 310965 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 70264-029-01 MOTRIN IB 50 in 1 BOX TABLET, FILM COATED 50 4 70264-029-01 MOTRIN IB 2 in 1 POUCH TABLET, FILM COATED 2 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70264-029 MOTRIN IB (IBUPROFEN) TABLET, FILM COATED [R J GENERAL CORPORATION] 3 Current NDC, Legacy NDC, 2 package rows 20241030_afa87bb5-7fcb-4ccd-acac-f7931242181f.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 58 of 79 · 1,570 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Acetaminophen ACETAMINOPHEN Kroger Company 5bfd9841-c781-43be-b823-d334893ae6ed 2024-10-24 Warnings Exact identifier application number: M013 Pain Relief ACETAMINOPHEN H E B add6952e-9dd5-487c-93e6-337e9d6a4872 2024-10-24 Warnings Exact identifier application number: M013 Dye Free Pain Reliever Childrens ACETAMINOPHEN Safeway, Inc. 7d55cb42-295f-473a-941d-71825b44a3c0 2024-10-24 Warnings Exact identifier application number: M013 rapid release pain relief ACETAMINOPHEN Publix Super Markets Inc d0b34133-d69d-47db-bf51-be942769c612 2024-10-24 Warnings Exact identifier application number: M013 basic care acetaminophen ACETAMINOPHEN Amazon.com Services LLC 00146b91-008d-4b16-95b0-6077f98821be 2024-10-24 Warnings Exact identifier application number: M013 equate pain reliever ACETAMINOPHEN WALMART INC. 9a20273e-a4d1-4c38-9efb-e6347f8dc14e 2024-10-24 Warnings Exact identifier application number: M013 Pain Relief Extra Strength ACETAMINOPHEN MARC GLASSMAN, INC. e221905b-a795-c067-e053-2a95a90a02e7 2024-10-23 Warnings Exact identifier application number: M013 Pain Relief PM Extra Strength ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE MARC GLASSMAN, INC. e221bbce-83de-0f03-e053-2995a90abca5 2024-10-23 Warnings Exact identifier application number: M013 Pain Relief Extra Strength ACETAMINOPHEN MARC GLASSMAN, INC. e231c2f6-927c-1ab0-e053-2995a90a6121 2024-10-23 Warnings Exact identifier application number: M013 Pain Relief Extra Strength ACETAMINOPHEN MARC GLASSMAN, INC. e23703bb-6087-7985-e053-2995a90aa5ec 2024-10-23 Warnings Exact identifier application number: M013 Pain Relief PM Extra Strength ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE MARC GLASSMAN, INC. e237550d-711d-5d87-e053-2995a90affce 2024-10-23 Warnings Exact identifier application number: M013 Aspirin ASPIRIN HARRIS TEETER a6f15f71-1327-4b71-b9d6-e3e9f0243801 2024-10-22 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN HARRIS TEETER 43308b23-7d4f-4e4f-a497-af71920d86aa 2024-10-22 Warnings Exact identifier application number: M013 Pain Relief Regular Strength ACETAMINOPHEN MARC GLASSMAN, INC. e21e821c-9694-5db0-e053-2995a90ad034 2024-10-22 Warnings Exact identifier application number: M013 Pain Relief Extra Strength ACETAMINOPHEN MARC GLASSMAN, INC. e21e90e8-b9f1-1133-e053-2995a90a664b 2024-10-22 Warnings Exact identifier application number: M013 aspirin ASPIRIN Publix Super Markets Inc c51dae48-aa49-4926-b04a-0da264e08dfa 2024-10-22 Warnings Exact identifier application number: M013 Acetaminophen Extra Strength ACETAMINOPHEN KROGER COMPANY b96a2280-ec4f-7c61-e053-2995a90a18bb 2024-10-22 Warnings Exact identifier application number: M013 Pain Relief Extra Strength ACETAMINOPHEN HEB f17a18b0-a7c2-4c64-868c-460cf34e1f7d 2024-10-21 Warnings Exact identifier application number: M013 Pain Relief Extra Strength ACETAMINOPHEN HEB 0863aeaa-15ec-4c67-ba79-4dad54555bd2 2024-10-21 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN American Health Packaging 3c0175a0-175b-48b8-9192-3f869690c0f2 2024-10-21 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 70264-029-01 70264002901 50 POUCH in 1 BOX (70264-029-01) / 2 TABLET, FILM COATED in 1 POUCH 50 pouch 2021-05-01 0000-00-00 No No Current