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 |
|---|---|---|---|---|---|---|
| Motion Sickness | DIMENHYDRINATE | CVS Pharmacy | 0998947c-cfba-497e-bf7a-9c7f8fff1764 | 2026-07-16 | Warnings | M009 |
| LEADER No Drip | ALLERGY SINUS NASAL MIST | CARDINAL HEALTH 110, LLC. DBA LEADER | e7b2c1c1-6250-4af3-b131-22aced2b23d5 | 2026-07-16 | Warnings | M012 |
| Mucus Relief DM Cough | DEXTROMETHORPHAN HBR, GUAIFENESIN | Amerisource Bergen | 639a59b7-ccff-485e-a232-38b680827229 | 2026-07-16 | Warnings | M012 |
| Acetaminophen Extra Strength | ACETAMINOPHEN | Dr. Reddy's Laboratories Inc. | 9d34abc2-3a9a-b68f-80d4-4ede1eb1e45f | 2026-07-15 | Warnings | M013 362O9ITL9D |
| Equate Nighttime Vapor Ice Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | WALMART INC. | 30470a01-4d42-44c6-a017-d68bb74cdef7 | 2026-07-15 | Warnings | M012 362O9ITL9D |
| Acetaminophen | ACETAMINOPHEN | Family Dollar, Inc. | 3f182571-3212-eb29-e063-6294a90a9fa0 | 2026-07-15 | Warnings | M013 362O9ITL9D |
| ibuprofen | IBUPROFEN | Sun Pharmaceutical Industries, Inc. | 9de61620-6750-4fb6-89a4-fe451ab8d99f | 2026-07-15 | Warnings | WK2XYI10QM |
| Simethicone | TARGET BERRY BLAST ANTACID HBG CHEW | Target | 5245af45-77c7-c95f-e063-6294a90a24f7 | 2026-07-15 | Warnings | M001 H0G9379FGK |
| Amazon Basics Cherry Antacid SC | CALCIUM CARBONATE | Amazon | 4b1d6e4e-8b59-ec06-e063-6394a90aa60d | 2026-07-15 | Warnings | M001 H0G9379FGK |
| Quality Choice Effervescent Cold Relief - Plus | ASPIRIN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE BITARTRATE | Chain Drug Marketing Association | 1f93fe6d-ee21-e323-e063-6394a90a61bf | 2026-07-15 | Warnings | M012 R16CO5Y76E |
| Pentrexcilina Daytime | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCL | OPMX LLC | b7b3c15a-bb28-5c25-e053-2a95a90ad3b1 | 2026-07-15 | Warnings | M012 04JA59TNSJ 362O9ITL9D |
| Quality Choice Effervescent Cold Relief - Orange | ASPIRIN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE BITARTRATE | Chain Drug Marketing Association | 1f93c815-63c7-bfe0-e063-6394a90ab4a5 | 2026-07-15 | Warnings | M012 R16CO5Y76E |
| FEVIA Acid Control | CALCIUM CARBONATE | VIVUNT PHARMA LLC | 4b1bd2d1-c909-f5db-e063-6394a90a84bc | 2026-07-15 | Warnings | M001 H0G9379FGK |
| FEVIA Acid Control | CALCIUM CARBONATE | VIVUNT PHARMA LLC | 4d695a90-6502-3020-e063-6394a90ab0c3 | 2026-07-15 | Warnings | M001 H0G9379FGK |
| FEVIA Diarrhea Control | BISMUTH SUBSALICYLATE | VIVUNT PHARMA LLC | 4bd5aa23-37aa-b818-e063-6394a90ae06c | 2026-07-15 | Warnings | M008 62TEY51RR1 |
| Allergy Relief | LORATADINE | Dr. Reddy's Laboratories Inc. | 44da36d2-1881-e779-d3a2-13ea828f9240 | 2026-07-15 | Warnings | 311372 7AJO3BO7QN |
| Aspirin | ASPIRIN | DOLGENCORP, LLC | 955484a6-2a7a-4b15-a9b4-e888ed5de04c | 2026-07-15 | Warnings | M013 212033 R16CO5Y76E |
| Stomach Relief | BISMUTH SUBSALICYLATE | WALMART INC. (see also Equate) | 369fe912-dd0e-4ff3-a597-5ee81332838a | 2026-07-15 | Warnings | M008 62TEY51RR1 |
| Ibuprofen | IBUPROFEN | Strides Pharma Science Limited | 38ebacc3-378f-483e-babc-76119677e7df | 2026-07-15 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Stomach Relief Ultra | BISMUTH SUBSALICYLATE | EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC) | 642c14bd-be99-410b-9ba7-6e71c9705230 | 2026-07-15 | Warnings | M008 62TEY51RR1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.