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 |
|---|---|---|---|---|---|---|
| Arthritis Pain | ACETAMINOPHEN | AMERIFOODS TRADING COMPANY | 3802bc07-3154-f36a-e063-6294a90ac1cc | 2025-11-20 | Warnings | 362O9ITL9D |
| GERI-MOX ANTACID ANTIGAS | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | Geri-Care Pharmaceuticals, Corp | 03358bc7-8819-4a05-bc13-27fbf486bd26 | 2025-11-20 | Warnings | M001 |
| Pain Relief | ACETAMINOPHEN | HYVEE INC | 4227aeb1-dd2c-9ca1-e063-6294a90ad709 | 2025-11-20 | Warnings | M013 362O9ITL9D |
| good sense pain relief | ACETAMINOPHEN | NuCare Pharamceuticals, Inc. | 440c13d7-edf0-f611-e063-6394a90af995 | 2025-11-20 | Warnings | M013 313782 362O9ITL9D |
| Pain Relief | ACETAMINOPHEN | HYVEE INC | 42394377-c874-a955-e063-6294a90ace0b | 2025-11-20 | Warnings | 362O9ITL9D |
| Pain Relief | ACETAMINOPHEN | HYVEE INC | 4227a2cc-69fa-869d-e063-6294a90a1d41 | 2025-11-20 | Warnings | M013 362O9ITL9D |
| Pain Relief | ACETAMINOPHEN | HYVEE INC | 422796ed-7558-f7e8-e063-6294a90ad1c7 | 2025-11-20 | Warnings | M013 362O9ITL9D |
| Arthritis Pain | ACETAMINOPHEN | HYVEE INC | 3e61b583-c1cb-23bd-e063-6294a90aa006 | 2025-11-20 | Warnings | 362O9ITL9D |
| Pain Relief | ACETAMINOPHEN | HYVEE INC | 3e61abe4-b4be-01af-e063-6394a90a8b24 | 2025-11-20 | Warnings | M013 362O9ITL9D |
| Pain Relief PM | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE | HYVEE INC | 3e60703b-a5cf-333a-e063-6394a90a2087 | 2025-11-20 | Warnings | M013 TC2D6JAD40 362O9ITL9D |
| Melox | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE | Belmora LLC | d41f0b26-5add-4045-9754-37d70d120d28 | 2025-11-20 | Warnings | M001 |
| Supress DX Pediatric Drops | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | KRAMER NOVIS | ddb95436-7806-4086-af4d-18a6625b5c83 | 2025-11-20 | Warnings | M012 04JA59TNSJ |
| SODIUM BICARBONATE | SODIUM BICARBONATE | Glenmark Pharmaceuticals Inc., USA | f38d0dfc-9bcc-4224-a202-885c9ad0beae | 2025-11-20 | Warnings, Adverse reactions | 8MDF5V39QO |
| Loperamide Hydrochloride 2mg | LOPERAMIDE HYDROCHLORIDE TABLETS USP, 2MG | MARKSANS PHARMA LIMITED | 644fb37a-1d97-4333-a5c7-5a485ab338f7 | 2025-11-19 | Warnings | 978010 77TI35393C |
| ALLERGY RELIEF-D | LORATADINE AND PSEUDOEPHEDRINE | CVS Pharmacy | 0b26004d-f741-48e1-bf2b-ec4af8150160 | 2025-11-19 | Warnings | 7AJO3BO7QN |
| Tums Chewy Bites Vanilla and Mint | CALCIUM CARBONATE | Haleon US Holdings LLC | 2b9dd909-c850-3c21-e063-6394a90a15a8 | 2025-11-19 | Warnings | M001 H0G9379FGK |
| WALGREENS EARACHE DROPS | BELLADONNA LEAF, CALCIUM CARBONATE, CHAMOMILE, LYCOPODIUM CLAVATUM SPORE, ANEMONE PATENS, AND SULFUR | Walgreen Company | c573dc3c-992e-604d-e053-2995a90a0ff4 | 2025-11-19 | Warnings | H0G9379FGK |
| MAXIMUM STRENGTH ANTACID ANTIGAS | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE | WALGREEN COMPANY | 7cd8fdf4-f762-f936-e053-2a91aa0aa6ee | 2025-11-19 | Warnings | M001 |
| SUPREME ANTACID | CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | FAMILY DOLLAR SERVICES INC | 5e996df3-25a4-b259-e053-2a91aa0a4311 | 2025-11-19 | Warnings | M001 H0G9379FGK |
| GERI-LANTA ANTACID ANTIGAS | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE | Geri-Care Pharmaceuticals, Corp | a7d7298f-44d6-4e09-8578-7fe311243002 | 2025-11-19 | Warnings | M001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.