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
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| SurviveX Travel Med Kit - Intent Brands LLC | Intent Brands LLC | 2026-05-07 | HUMAN OTC DRUG LABEL |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Nighttime Sleep Aid | DIPHENHYDRAMINE HCL | Care One (Retail Business Services, LLC.) | 51e633a8-5bfc-4ff9-816f-3bc22b8a5c4c | 2025-05-23 | Warnings | TC2D6JAD40 |
| Nighttime Sleep Aid Maximum Strength | DIPHENHYDRAMINE HCL | Care One (Retail Business Services, LLC.) | 536cd7d6-a470-4614-89c8-6c3ada582a90 | 2025-05-23 | Warnings | TC2D6JAD40 |
| equate ibuprofen childrens | IBUPROFEN | Wal-Mart Stores Inc | ed9ee7b5-2d9a-4aaf-a245-aa13fcc6365a | 2025-05-23 | Warnings | WK2XYI10QM |
| Pain Relief | ACETAMINOPHEN | CHAIN DRUG MARKETING ASSOCIATION, INC. | 1c083e29-8732-4ecd-ab4b-9038acbd0b9d | 2025-05-22 | Warnings | M013 362O9ITL9D |
| ibuprofen | IBUPROFEN | Bryant Ranch Prepack | 92878aad-0bf9-4303-a1f8-4b9b23848a71 | 2025-05-21 | Warnings | WK2XYI10QM |
| Loratadine Allergy Relief | LORATADINE | Asclemed USA, Inc. | 332bda00-1350-2d33-e063-6394a90a8bd7 | 2025-05-21 | Warnings | ANDA076134 311372 7AJO3BO7QN |
| MAXIMUM STRENGTH COLD AND FLU | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | TARGET CORP | 9dfef3dc-dbc8-659a-e053-2995a90a8c3b | 2025-05-21 | Warnings | M012 04JA59TNSJ 362O9ITL9D |
| TYLENOL For Children Plus Adults | ACETAMINOPHEN | Kenvue Brands LLC | 5bb8ef99-a94b-49f9-89f9-cd1ce0a47a42 | 2025-05-21 | Warnings | M013 362O9ITL9D |
| Anti-Diarrheal | LOPERAMIDE HYDROCHLORIDE | CHAIN DRUG MARKETING ASSOCIATION INC. | 35a938af-decf-5b5d-e063-6294a90a9ab0 | 2025-05-21 | Warnings | 77TI35393C |
| Anti-Diarrheal | LOPERAMIDE HYDROCHLORIDE | CHAIN DRUG MARKETING ASSOCIATION INC. | 35aa2daf-3486-7ee2-e063-6394a90ad473 | 2025-05-21 | Warnings | 77TI35393C |
| Ibuprofen | IBUPROFEN | NuCare Pharmaceuticals, Inc. | 2c3f8149-9b77-54cd-e063-6394a90a847e | 2025-05-21 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| childrens ibuprofen | IBUPROFEN | CVS Pharmacy | 884d51d8-4774-4dde-b854-32abfb4b712d | 2025-05-20 | Warnings | WK2XYI10QM |
| Diphenhydramine HCl | DIPHENHYDRAMINE HCL | BI-MART | 2914504a-ed42-4168-9e5c-f49407ed5a30 | 2025-05-20 | Warnings | TC2D6JAD40 |
| Adult Tussin | GUAIFENESIN | Camber Consumer Care | 896d2540-279a-4405-b176-acbff56303e5 | 2025-05-20 | Warnings | M012 |
| Nuvicare NightTime Cold and Flu Softgel | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | NUVICARE LLC | 37a88914-6234-4191-86f5-103c396c52af | 2025-05-20 | Warnings | M012 362O9ITL9D |
| Nuvicare DayTime Cold and Flu Softgel | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | NUVICARE LLC | 1ea15426-4f3d-4a97-a590-6bd73bc6cbcd | 2025-05-19 | Warnings | M012 04JA59TNSJ 362O9ITL9D |
| Theraflu Flu Relief Max Strength Daytime Nighttime Combo Pack | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, AND ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR | Haleon US Holdings LLC | 812a093f-cf83-4f7a-927a-1b5695be7f90 | 2025-05-19 | Warnings | M012 |
| Acetaminophen and Ibuprofen | ACETAMINOPHEN AND IBUPROFEN | Meijer Distribution Inc | 2d916b1b-334f-15c7-e063-6294a90ae8b4 | 2025-05-19 | Warnings | WK2XYI10QM 362O9ITL9D |
| equate dual back pain reliever | ACETAMINOPHEN, IBUPROFEN | WALMART INC. | af7e6478-177f-473d-9d14-1e78610b1a6e | 2025-05-17 | Warnings | WK2XYI10QM 362O9ITL9D |
| MUCUS RELIEF | GUAIFENESIN | SDA Laboratories, Inc. | 1fd16b06-0c3e-4a30-ae6a-7b1632189c20 | 2025-05-16 | Warnings | M012 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.