Home NDC 87625-104 NDC 87625-104 - 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 87625-104
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 141 of 485 · 9,690 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Chewable Aspirin 81 mg ASPIRIN HYVEE INC 459f749f-9d23-8752-e063-6394a90a8c81 2026-01-13 Warnings Exact identifier application number: M013 unii: R16CO5Y76E Severe Cold and Flu ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE HYVEE INC 462cbf3d-51b1-dab9-e063-6394a90a70ba 2026-01-13 Warnings Exact identifier application number: M012 unii: 04JA59TNSJ unii: 362O9ITL9D Ibuprofen IBUPROFEN HYVEE INC 45aead8a-37ee-9a66-e063-6394a90a5d17 2026-01-13 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM Rest Simply DIPHENHYDRAMINE HYDROCHLORIDE HYVEE INC 462ca6cd-8eec-09df-e063-6294a90ac880 2026-01-13 Warnings Exact identifier rxcui: 1049630 unii: TC2D6JAD40 ASPIRIN 325 mg ASPIRIN HYVEE INC 459d01df-6ff6-cff6-e063-6394a90ab35c 2026-01-13 Warnings Exact identifier application number: M013 rxcui: 212033 unii: R16CO5Y76E Ibuprofen IBUPROFEN HYVEE INC 459fc063-0664-09b7-e063-6394a90a89e0 2026-01-13 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM Ibuprofen IBUPROFEN HYVEE INC 459fc670-32a3-61a6-e063-6294a90aea5a 2026-01-13 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM Pocket Farmacy MENTHOL Saje Natural Business Inc. 4260542e-0980-4b0b-8177-1c9f2c53b5a6 2026-01-13 Warnings Exact identifier application number: M012 Sweet Comfort MENTHOL Saje Natural Business Inc. cf13cccd-723d-4d61-8a5e-b36281605cc7 2026-01-13 Warnings Exact identifier application number: M012 Fortify MENTHOL Saje Natural Business Inc. 0320a305-99d1-4909-94cc-cd6509ecb948 2026-01-13 Warnings Exact identifier application number: M012 Rolling Farmacy MENTHOL Saje Natural Business Inc. a38765a9-22cd-4fc5-b5ab-c3cacbd52c74 2026-01-13 Warnings Exact identifier application number: M012 Home Farmacy MENTHOL Saje Natural Business Inc. add35d10-b27a-4ae8-b2de-8a285aaef155 2026-01-13 Warnings Exact identifier application number: M012 Traveling Farmacy MENTHOL Saje Natural Business Inc. 5b70f5aa-ed36-65ab-e053-2a91aa0a6777 2026-01-13 Warnings Exact identifier application number: M012 Ibuprofen IBUPROFEN L.N.K. International, Inc. 8ebe3e16-b7ae-d333-6671-5bc935e25900 2026-01-13 Warnings Exact identifier rxcui: 310965 unii: WK2XYI10QM equaline complete dual action FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE United Natural Foods, Inc. dba UNFI c32cb5be-e1f8-4510-8685-5e03a7d4224c 2026-01-13 Warnings Exact identifier unii: H0G9379FGK ibuprofen IBUPROFEN HyVee Inc 2fd51545-1d1f-4b2e-a084-d28ba223e720 2026-01-13 Warnings Exact identifier unii: WK2XYI10QM anti diarrheal LOPERAMIDE HYDROCHLORIDE HyVee Inc 9434cefe-6b13-47c4-b2f7-b8d566c5a4ff 2026-01-13 Warnings Exact identifier rxcui: 978010 unii: 77TI35393C sinus plus allergy PE maximum strength CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCL United Natural Foods, Inc. dba UNFI 660d3c80-f249-41dd-aa93-a0b1e635ead0 2026-01-13 Warnings Exact identifier application number: M012 unii: 04JA59TNSJ ibuprofen infants IBUPROFEN HyVee Inc e8fcaf17-234a-4d64-b621-9ca505884b0a 2026-01-12 Warnings Exact identifier unii: WK2XYI10QM Pain Terminator Extra Strength Pain Relief CAFFEINE, ACETAMINOPHEN, ASPIRIN Wildman Business Group 8ffb02d9-92df-4d2f-a367-1c71490807fb 2026-01-12 Warnings Exact identifier application number: M013 unii: R16CO5Y76E unii: 362O9ITL9D
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.