Home NDC 87625-110 NDC 87625-110 - 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 87625-110
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 164 of 487 · 9,734 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Loratadine LORATADINE GRANULES USA, INC. c3c9bc45-7ed5-abf4-e053-2995a90a40ff 2025-12-22 Warnings Exact identifier rxcui: 311372 unii: 7AJO3BO7QN Acetaminophen ACETAMINOPHEN Granules USA, Inc. 96131c7b-bdff-0642-e053-2a95a90a4f32 2025-12-22 Warnings Exact identifier unii: 362O9ITL9D Acetaminophen Diphenhydramine HCl ACETAMINOPHEN DIPHENHYDRAMINE HCL Granules USA, Inc. 8c9f68e3-fedc-6457-e053-2995a90a045a 2025-12-22 Warnings Exact identifier application number: M013 unii: TC2D6JAD40 unii: 362O9ITL9D Loratadine antihistamine LORATADINE NCS HealthCare of KY, LLC dba Vangard Labs f3d05276-21bd-419d-8dba-07ce278d3375 2025-12-22 Warnings Exact identifier rxcui: 311372 unii: 7AJO3BO7QN BASIC CARE DAYTIME NIGHTTIME SEVERE COLD AND FLU ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE Amazon.com Services LLC 82e68c65-9898-4106-a2f8-e39d124c703e 2025-12-22 Warnings Exact identifier application number: M012 Nighttime Cold and Flu Relief ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE Harris Teeter, LLC 89fd57d2-fe49-41cb-b02e-9643e526cf47 2025-12-22 Warnings Exact identifier application number: M012 unii: 362O9ITL9D Aspirin ASPIRIN L.N.K. International, Inc. 35005045-57b2-4ffe-ab70-22d570c1b161 2025-12-22 Warnings Exact identifier application number: M013 rxcui: 212033 unii: R16CO5Y76E Menthol Cough Drop MENTHOL Walgreens 464f6645-ca33-1722-e054-00144ff8d46c 2025-12-21 Warnings Exact identifier application number: M012 Cherry Cough Drops MENTHOL Walgreen Co. 47f38e79-c730-21b9-e054-00144ff88e88 2025-12-21 Warnings Exact identifier application number: M012 Cherry Cough Drop MENTHOL Walgreen Co. 47522852-005a-2a66-e054-00144ff8d46c 2025-12-21 Warnings Exact identifier application number: M012 Honey Lemon Cough Drop MENTHOL Walgreens Co, 47653657-80b5-482f-e054-00144ff88e88 2025-12-21 Warnings Exact identifier application number: M012 Honey Lemon Cough Drop MENTHOL Walgreen Co. 47f89d33-6e0a-4bb4-e054-00144ff88e88 2025-12-21 Warnings Exact identifier application number: M012 Strawberry Cough Drop MENTHOL 2.7 MG Walgreen Co. 4766afa8-fdaf-05e5-e054-00144ff8d46c 2025-12-21 Warnings Exact identifier application number: M012 SF Menthol Cough Drop MENTHOL Walgreen Co. 477b9fc3-c3c5-647e-e054-00144ff8d46c 2025-12-21 Warnings Exact identifier application number: M012 SF Honey Lemon Cough Drop MENTHOL Walgreen Co. 477cedee-6bd3-2a34-e054-00144ff8d46c 2025-12-21 Warnings Exact identifier application number: M012 Cherry Sore Throat Lozenge BENZOCAINE Walgreens Co. 47e0f809-0b30-2b23-e054-00144ff8d46c 2025-12-21 Warnings Exact identifier application number: M012 Antacid Soft Chew CALCIUM CARBONATE Walgreen Co. 479284ad-ec02-4b74-e054-00144ff8d46c 2025-12-21 Warnings Exact identifier application number: M001 unii: H0G9379FGK Antacid Flavor Chew CALCIUM CARBONATE Walgreen Co. 47dfbe23-f407-6588-e054-00144ff8d46c 2025-12-21 Warnings Exact identifier application number: M001 unii: H0G9379FGK Antacid Flavor Chews CALCIUM CARBONATE Walgreen Co. 47e0830f-31e7-5ff0-e054-00144ff88e88 2025-12-21 Warnings Exact identifier application number: M001 unii: H0G9379FGK Sugar Free Honey Lemon Cough Drops MENTHOL Walgreen 835e276a-493e-1038-e053-2a91aa0a7ea2 2025-12-21 Warnings Exact identifier application number: M012
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.