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 216 of 483 · 9,642 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ultra Strength CALCIUM CARBONATE BETTER LIVING BRANDS LLC 35b3d9d0-b04d-4f6d-b99d-435233803d4b 2025-10-29 Warnings Exact identifier application number: M001 unii: H0G9379FGK Ultra Strength ANTACID TABLETS SAFEWAY 4c6cdd81-5145-4a1f-888f-85cf5d856c39 2025-10-29 Warnings Exact identifier application number: M001 unii: H0G9379FGK Extra Strength Smooth ANTACID TABLETS SAFEWAY 8ed35c3b-9878-4889-90f7-a3973cf806e0 2025-10-29 Warnings Exact identifier application number: M001 unii: H0G9379FGK Maximum Strength Severe Congestion and Cough DEXTROMETHORPHAN HBR, GUAIFENESIN, AND PHENYLEPHRINE HCL SAFEWAY 013b94a1-26c7-4371-981a-d1b9d7fd1c98 2025-10-29 Warnings Exact identifier application number: M012 unii: 04JA59TNSJ Stomach Relief BISMUTH SUBSALICYLATE SAFEWAY ba698d38-83f1-4257-9c43-e7a55dbb206e 2025-10-29 Warnings Exact identifier application number: M008 rxcui: 308761 unii: 62TEY51RR1 Digestive Relief BISMUTH SUBSALICYLATE SAFEWAY 5538d56a-b258-4260-b51b-f5131bd76885 2025-10-29 Warnings Exact identifier application number: M008 unii: 62TEY51RR1 Better Living PHENYLEPHRINE HYDROCHLORIDE BETTER LIVING BRANDS LLC aea0db7f-e01a-4d8e-9c20-4a5ef4a905d1 2025-10-29 Warnings Exact identifier application number: M012 unii: 04JA59TNSJ MAPAP Extra Strength ACETAMINOPHEN Major Pharmaceuticals 34a95450-3f04-4de4-9113-73e7bd5724a0 2025-10-29 Warnings Exact identifier application number: M013 unii: 362O9ITL9D KOSHER MEDS IBUPROFEN Mollec Inc c9c31326-6a19-9a9c-e053-2a95a90aed06 2025-10-29 Warnings Exact identifier unii: WK2XYI10QM Kosher Meds Dye-Free Ibuprofen IBUPROFEN Mollec Inc ba1a0bc2-0a28-4d73-9667-5a220b806e87 2025-10-29 Warnings Exact identifier unii: WK2XYI10QM AXIM DayTime - Night Time 72 Softgels ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE VIVUNT PHARMA LLC de9eb2d5-ba51-4637-e053-2995a90a0451 2025-10-29 Warnings Exact identifier application number: M012 Dollar General Vapor Steam CAMPHOR (SYNTHETIC) DOLGENCORP, LLC 86d0f3ac-1359-c2f9-e053-2a91aa0a35d0 2025-10-29 Warnings Exact identifier application number: M012 hemorrhoidal GLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUM Publix Super Markets Inc 354a640c-bc7e-45c8-9df0-8b5b01767f5c 2025-10-29 Warnings Exact identifier unii: 04JA59TNSJ GOODNOW SLEEP AID DIPHENHYDRAMINE HCL Gobrands, Inc 7d821b7d-6a31-4ff7-b587-51907ba62658 2025-10-29 Warnings Exact identifier unii: TC2D6JAD40 GOODNOW PAIN RELIEF ACETAMINOPHEN Gobrands, Inc 4d4a78a5-5a88-4f24-b685-c7c6bb5e989e 2025-10-29 Warnings Exact identifier application number: M013 unii: 362O9ITL9D All Day Allergy Relief LORATADINE Family Dollar (FAMILY WELLNESS) 6b8d786e-2ee3-487f-bf7b-7dc738ea2fc9 2025-10-29 Warnings Exact identifier rxcui: 311372 unii: 7AJO3BO7QN Hydrocodone Bitartrate and Acetaminophen HYDROCODONE BITARTRATE AND ACETAMINOPHEN Amneal Pharmaceuticals of New York LLC e0cefc7b-e81c-4e15-89a0-fe71dc94338b 2025-10-28 Boxed warning, Warnings, Adverse reactions Exact identifier unii: 362O9ITL9D Up and Up Childrens Ibuprofen IBUPROFEN Target Corporation 17b3ca97-1bd6-4e76-a47f-2e35ef36b707 2025-10-28 Warnings Exact identifier unii: WK2XYI10QM childrens ibuprofen 100 IBUPROFEN Walgreen Company 7b798146-393f-422c-87f0-0bf800df0c71 2025-10-28 Warnings Exact identifier unii: WK2XYI10QM Maximum Strength Mucus Relief DM DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN Wal-Mart Stores,Inc., a748d5ab-901c-47bb-8437-997542ecebfe 2025-10-28 Warnings Exact identifier application number: M012
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.