Home NDC 87625-113 NDC 87625-113 - SurviveX Travel Med MOD 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 87625-113
Manufacturer Intent Brands LLC
Effective date 2026-08-04
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 172 of 481 · 9,620 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Meijer Severe Menthol Throat Drops MENTHOL Meijer 16603ca4-1ce5-2e7e-e063-6394a90ad6f1 2025-12-18 Warnings Exact identifier application number: M012 Meijer Max Gas 30ct SIMETHICONE Meijer 23f95dcf-3d4c-a119-e063-6394a90a5155 2025-12-18 Warnings Exact identifier application number: M001 unii: H0G9379FGK Meijer Bismuth Stomach Relief BISMUTH Meijer 26a65c79-3bc1-a424-e063-6394a90a848e 2025-12-18 Warnings Exact identifier application number: M008 rxcui: 308761 unii: 62TEY51RR1 Ibuprofen IBUPROFEN A-S Medication Solutions e5db46f3-043b-40ac-a89b-c90bd562e7b4 2025-12-18 Boxed warning, Warnings, Adverse reactions Exact identifier unii: WK2XYI10QM DRAMAMINE MECLIZINE HYDROCHLORIDE Medtech Products Inc. 6efd3473-ee14-4ee0-8a58-d15a64a9224a 2025-12-18 Warnings Exact identifier application number: M009 unii: HDP7W44CIO Allergy Relief Childrens DIPHENHYDRAMINE HCL A-S Medication Solutions 60587987-c303-4617-ba96-c518ab2a0650 2025-12-18 Warnings Exact identifier application number: M012 unii: TC2D6JAD40 Acetaminophen ACETAMINOPHEN Caplin Steriles Limited b6f83919-8608-4648-9ac6-e13eadac8404 2025-12-18 Boxed warning, Warnings, Adverse reactions Exact identifier unii: 362O9ITL9D Pain and Fever Childrens ACETAMINOPHEN CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED e55645ab-66f9-4160-8247-395bc5b02711 2025-12-18 Warnings Exact identifier application number: M013 unii: 362O9ITL9D Hydrocodone Bitartrate and Acetaminophen HYDROCODONE BITARTRATE AND ACETAMINOPHEN Aurolife Pharma, LLC 392a846e-7325-462d-b19b-8afda44c5cb0 2025-12-17 Boxed warning, Warnings, Adverse reactions Exact identifier unii: 362O9ITL9D Antacid Regular strength ANTACID TABLETS WALGREEN CO. 9090e2c0-4837-44ea-b6c4-f46532eadee1 2025-12-17 Warnings Exact identifier application number: M001 unii: H0G9379FGK Dolex Forte ACETAMINOPHEN, ASPIRIN, CAFFEINE Pharmadel LLC 3c2d90fc-130d-476c-e063-6294a90a8c15 2025-12-17 Warnings Exact identifier application number: M013 unii: R16CO5Y76E unii: 362O9ITL9D Niaflu DEXTROMETHORPHAN HBR, GUAIFENESIN Pharmadel LLC 399898f0-e40a-4f5d-e063-6294a90a667d 2025-12-17 Warnings Exact identifier application number: M012 Cherry cough drop MENTHOL The Kroget Co. 4313a6ce-454d-4c4b-e054-00144ff88e88 2025-12-17 Warnings Exact identifier application number: M012 Menthol cough drop MENTHOL The Kroger Co. 42b257e9-f45e-32c9-e054-00144ff8d46c 2025-12-17 Warnings Exact identifier application number: M012 Honey Lemon cough drop MENTHOL The Kroger Co. 4318f25a-05d9-2208-e054-00144ff88e88 2025-12-17 Warnings Exact identifier application number: M012 Honey Lemon cough drop MENTHOL The Kroger Co. 4317f952-a228-0281-e054-00144ff88e88 2025-12-17 Warnings Exact identifier application number: M012 Honey Lemon Cough Drop MENTHOL The Kroger Co. 4316df6e-3ae6-4ab5-e054-00144ff88e88 2025-12-17 Warnings Exact identifier application number: M012 SF Honey Lemon Cough Drops MENTHOL The Kroger Co. 43281bd1-f8a7-02a4-e054-00144ff8d46c 2025-12-17 Warnings Exact identifier application number: M012 Kroger Cherry Cough Drops MENTHOL Kroger a2e1d1f5-9b19-1704-e053-2a95a90abb51 2025-12-17 Warnings Exact identifier application number: M012 Kroger Cherry Antacid Soft Chew CALCIUM CARBONATE Kroger 142d7c79-f87f-03fd-e063-6394a90adb0b 2025-12-17 Warnings Exact identifier application number: M001 unii: H0G9379FGK
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.