Home NDC 87625-101 NDC 87625-101 - SurviveX Travel Med Kit This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 87625-101
Manufacturer Intent Brands LLC
Effective date 2026-05-07
Current FDA listing Not matched in FDA.report NDC product tables 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 166 of 486 · 9,714 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Kaopectate Max Peppermint Flavor Anti Diarrheal BISMUTH SUBSALICYLATE Kramer Laboratories e7218045-a593-485b-a5ba-03f3b35cbec4 2025-12-19 Warnings Exact identifier application number: M008 unii: 62TEY51RR1 MUCUS RELIEF GUAIFENESIN 400 MG NUVICARE LLC e25b440e-f389-443f-b333-c66ad1747158 2025-12-19 Warnings Exact identifier application number: M012 Cold and Flu severe ACETAMINOPHEN,DEXTROMETHORPHAN HBR,GUAIFENESIN,PHENYLEPHRINE HCL Wal-Mart Stores Inc 9fca25dc-f63e-487a-8b7c-84d65ea51cb5 2025-12-19 Warnings Exact identifier application number: M012 unii: 04JA59TNSJ unii: 362O9ITL9D Cold and Flu Severe ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL Geiss, Destin & Dunn Inc. a7d2eaee-484e-43aa-8ae3-0e050219383f 2025-12-19 Warnings Exact identifier application number: M012 unii: 04JA59TNSJ unii: 362O9ITL9D Tension Headache Relief ACETAMINOPHEN, CAFFEINE NUVICARE LLC ea4e50e9-2c4d-4e58-b2cb-ab23e91fd50e 2025-12-19 Warnings Exact identifier application number: M013 unii: 362O9ITL9D Acetaminophen ACETAMINOPHEN WAL-MART STORES INC 940936ac-e59f-7489-e053-2a95a90a6364 2025-12-19 Warnings Exact identifier unii: 362O9ITL9D Acetaminophen ACETAMINOPHEN WAL-MART STORES INC e34d07b5-ccbb-cd14-e053-2a95a90a394b 2025-12-19 Warnings Exact identifier unii: 362O9ITL9D Acetaminophen and Ibuprofen ACETAMINOPHEN AND IBUPROFEN WAL-MART STORES INC. 0aaddde9-4317-a828-e063-6294a90a26d5 2025-12-19 Warnings Exact identifier unii: WK2XYI10QM unii: 362O9ITL9D Naproxen Sodium Diphenhydramine HCL NAPROXEN SODIUM DIPHENHYDRAMINE HCL Walmart fe810c0e-ab42-5a8a-e053-6394a90affe4 2025-12-19 Warnings Exact identifier unii: TC2D6JAD40 Acetaminophen ACETAMINOPHEN Walmart 175495fd-c561-f813-e063-6294a90aac80 2025-12-19 Warnings Exact identifier application number: M013 unii: 362O9ITL9D Acetaminophen ACETAMINOPHEN WALMART INC 21b22e9f-b6d1-1819-e063-6294a90ae09c 2025-12-19 Warnings Exact identifier application number: M013 unii: 362O9ITL9D Acetaminophen and Diphenhydramine HCL ACETAMINOPHEN AND DIPHENHYDRAMINE HCL SAFEWAY f18c1aa2-5f8b-5458-e053-2995a90ab947 2025-12-19 Warnings Exact identifier application number: M013 unii: 362O9ITL9D Cherry Cough Drops MENTHOL Publix 66d8e5f7-9766-57f3-e053-2991aa0a7e17 2025-12-19 Warnings Exact identifier application number: M012 Honey Lemon Cough Drops MENTHOL Publix 66e89fa3-ee09-1d16-e053-2a91aa0ae17c 2025-12-19 Warnings Exact identifier application number: M012 Loratadine LORATADINE Safeway, Inc f2a2a754-0170-e37c-e053-2a95a90a4dca 2025-12-19 Warnings Exact identifier rxcui: 311372 unii: 7AJO3BO7QN Acetaminophen, Aspirin and Caffeine ACETAMINOPHEN, ASPIRIN AND CAFFEINE Safeway, Inc f2a2cbb5-5a63-7514-e053-2995a90a572c 2025-12-19 Warnings Exact identifier unii: R16CO5Y76E unii: 362O9ITL9D Acetaminophen ACETAMINOPHEN MEIJER DISTRIBUTION INC ed23c587-7806-1f64-e053-2a95a90aea7f 2025-12-19 Warnings Exact identifier unii: 362O9ITL9D Ibuprofen IBUPROFEN Retail Business Services, LLC 04115ec1-ef31-1746-e063-6394a90a0a52 2025-12-19 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM Ibuprofen IBUPROFEN RETAIL BUSINESS SERVICES,LLC. a567dc6f-bd83-b9f5-e053-2995a90a05ee 2025-12-19 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM Acetaminophen ACETAMINOPHEN MEIJER, INC. ed25620f-e39b-e30c-e053-2995a90af621 2025-12-19 Warnings Exact identifier unii: 362O9ITL9D
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.