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 |
|---|---|---|---|---|---|---|
| Extra Strength Acetaminophen | ACETAMINOPHEN | Hi-Tech Nutraceuticals, LLC | a36be487-7a36-550f-e053-2a95a90a95c1 | 2026-07-06 | Warnings | M013 362O9ITL9D |
| Acetaminophen | ACETAMINOPHEN | Hi-Tech Nutraceuticals, LLC | a39c524e-c131-d7fb-e053-2995a90a785b | 2026-07-06 | Warnings | M013 313782 362O9ITL9D |
| Theraflu Severe Cold Relief Daytime | ACETAMINOPHEN, DEXTROMETHORPHAN HBR | Select Consumer Group | 55fc7d6f-cc44-b4c0-e063-6294a90ae4fc | 2026-07-06 | Warnings | M012 362O9ITL9D |
| PAIN RELIEVER | ASPIRIN 81 MG | Health Pharma USA, LLC | d60aed37-3a9e-46d1-e053-2995a90a1d1f | 2026-07-06 | Warnings | M013 R16CO5Y76E |
| Magnesium Oxide | MAGNESIUM OXIDE | Westminster Pharmaceuticals, LLC | 52eeac0e-94bb-48c3-81dc-578e96406c01 | 2026-07-06 | Warnings | M001 |
| Loratadine | LORATADINE ORAL | KROGER COMPANY | b963d83b-584f-c447-e053-2995a90ad973 | 2026-07-06 | Warnings | 7AJO3BO7QN |
| Ibuprofen | IBUPROFEN | Better Living Brands, LLC | 45520969-7a2d-4469-ba25-7db160d50ccf | 2026-07-06 | Warnings | 310965 WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Preferred Pharmaceuticals Inc. | c0156053-add5-4bd5-b89f-f90df2e73be4 | 2026-07-06 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Allergy Plus Sinus Headache | ACETAMINOPHEN, DIPHENHYDRAMINE HCL AND PHENYLEPHRINE HCL | DOLGENCORP, LLC | f2eacb1b-8b29-41ec-828a-c1f902ac0934 | 2026-07-06 | Warnings | M012 04JA59TNSJ TC2D6JAD40 362O9ITL9D |
| Diphenhydramine hydrochloride | DIPHENHYDRAMINE HYDROCHLORIDE | Camber Pharmaceuticals, Inc. | f808ee14-fccf-4abe-b53a-a40b0b3bba03 | 2026-07-04 | Warnings, Adverse reactions | TC2D6JAD40 |
| Pepcid Complete | FAMOTIDINE, CALCIUM CARBONATE, AND MAGNESIUM HYDROXIDE | Select Consumer Group | 55cc3304-9094-3da8-e063-6394a90aa49b | 2026-07-04 | Warnings | H0G9379FGK |
| ADVIL DUAL ACTION WITH ACETAMINOPHEN | IBUPROFEN, ACETAMINOPHEN | Select Consumer Group | 55cd65fc-91bf-4979-e063-6294a90ab9b7 | 2026-07-04 | Warnings | WK2XYI10QM 362O9ITL9D |
| Tylenol PM Extra Strength | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE | Select Consumer Group | 55d0dceb-c9a9-778e-e063-6294a90a2ad7 | 2026-07-04 | Warnings | M013 TC2D6JAD40 362O9ITL9D |
| Benadryl | DIPHENHYDRAMINE HYDROCHLORIDE | Select Consumer Group | 55d10292-e673-9896-e063-6294a90a5674 | 2026-07-04 | Warnings | M012 1049630 TC2D6JAD40 |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | 20078671-536f-4b0b-a079-f90ac186a670 | 2026-07-03 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| MECLIZINE HYDROCHLORIDE | MECLIZINE HYDROCLORIDE | REMEDYREPACK INC. | ba2fb6de-af86-4c05-9018-135e1f8594f9 | 2026-07-03 | Warnings, Adverse reactions | 995666 HDP7W44CIO |
| Bayer Genuine Aspirin | ASPIRIN | Select Consumer Group | 3ca776c2-47ed-5107-e063-6394a90ac5df | 2026-07-03 | Warnings | M013 212033 R16CO5Y76E |
| ADVIL | IBUPROFEN | Select Consumer Group | 3ca752d8-957c-21b4-e063-6294a90a5285 | 2026-07-03 | Warnings | NDA018989 153008 310965 WK2XYI10QM |
| Advil Liquigel | IBUPROFEN | Select Consumer Group | 3ca6bc9d-090f-e412-e063-6394a90a6876 | 2026-07-03 | Warnings | WK2XYI10QM |
| Midol Complete | ACETAMINOPHEN, CAFFEINE, AND PYRILAMINE MALEATE | Select Consumer Group | 3ca96ed9-d9af-dbfe-e063-6394a90a2932 | 2026-07-03 | Warnings | 362O9ITL9D |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.