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
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| SurviveX Travel Med MOD - Intent Brands LLC | Intent Brands LLC | 2026-08-04 | HUMAN OTC DRUG LABEL |
| 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 |
|---|---|---|---|---|---|---|
| Sleep-Aid | DIPHENHYDRAMINE HCL | WALMART INC. (see also Equate) | 84c37f4d-60f6-490e-ba8b-47d1257fa6f8 | 2026-02-13 | Warnings | TC2D6JAD40 |
| Ibuprofen Childrens | IBUPROFEN | Major Pharmaceuticals | 9d56e64d-7860-4fd1-88d2-c537e50079d8 | 2026-02-13 | Warnings | WK2XYI10QM |
| nasal | PHENYLEPHRINE HYDROCHLORIDE | Kroger Company | 1c3dc4e6-452b-4c84-b53c-426cf9ae8f03 | 2026-02-12 | Warnings | M012 04JA59TNSJ |
| Nighttime Cold and Flu Relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE | United Natural Foods, Inc. dba UNFI | af42d3f7-661e-4322-aefe-2b7f9f1010d6 | 2026-02-12 | Warnings | M012 362O9ITL9D |
| Childrens Giltuss D | CHILDRENS GILTUSS D | Gil Pharmaceutical Corp | cfc2493b-e99e-4b55-98a9-053f95d49844 | 2026-02-12 | Warnings | M012 04JA59TNSJ |
| Giltuss D | GILTUSS D | Gil Pharmaceutical Corp | 298f5457-a7df-474d-9854-68918ee3d330 | 2026-02-12 | Warnings | M012 04JA59TNSJ |
| Aflora | MULTIVITAMIN | Oncora Pharma, LLC | 38e463d1-f608-7cb5-e063-6294a90a4abb | 2026-02-12 | Warnings, Adverse reactions | H0G9379FGK |
| Folixia | MULTIVITAMIN | Oncora Pharma, LLC | 413945b5-116b-d8b6-e063-6394a90a55e8 | 2026-02-12 | Warnings, Adverse reactions | H0G9379FGK |
| Nutralyn | MULTIVITAMIN | Oncora Pharma, LLC | 33da017b-1e8c-d41c-e063-6394a90aab8c | 2026-02-12 | Warnings, Adverse reactions | H0G9379FGK |
| Folaten | MULTIVITAMIN | Oncora Pharma, LLC | 93086235-2c33-424d-b0c3-213031988581 | 2026-02-12 | Warnings, Adverse reactions | H0G9379FGK |
| Vaporizing | CAMPHOR | Walgreen Co. | ef4f95c8-7650-4096-9369-ea8393781bee | 2026-02-12 | Warnings, Adverse reactions | M012 |
| Pain Reliever / Low Dose Aspirin | ASPIRIN | PHARMAMED USA INC | 1a3ff0da-85eb-542c-e063-6294a90a9cca | 2026-02-12 | Warnings | R16CO5Y76E |
| naproxen sodium pm | DIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUM | H E B | 4281faf5-7182-404f-9f53-3d9ea0354a18 | 2026-02-12 | Warnings | TC2D6JAD40 |
| Treda Ultra | BISMUTH SUBSALICYLATE | Laboratorios Sanfer, S.A. de C.V. | cfa7f37a-e18b-4929-b3a4-4126b0aa679a | 2026-02-12 | Warnings | M008 62TEY51RR1 |
| ASPIRIN Low Strength | ASPIRIN | CVS Pharmacy | 6e1c1129-562b-4a8a-ac37-db3cb2a82735 | 2026-02-11 | Warnings | M013 R16CO5Y76E |
| Oxymetazoline hydrochloride | OXYMETAZOLINE HYDROCHLORIDE | Prodose, Inc. | 3dce34f0-9f6d-8151-e063-6394a90a1d38 | 2026-02-11 | Warnings | M012 |
| CVS Acetaminophen | ACETAMINOPHEN | CVS Pharmacy | 3dd21aaf-13b2-9e81-e063-6294a90afaec | 2026-02-11 | Warnings | M013 362O9ITL9D |
| childrens ibuprofen | IBUPROFEN | HyVee Inc | d522a3ac-dd43-4faa-b3f8-69313be1c829 | 2026-02-11 | Warnings | WK2XYI10QM |
| SIGNATURE CARE Childrens Multi Symptom Cold | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | SAFEWAY | 831da7b6-25c7-4601-b7f1-1800a238b016 | 2026-02-11 | Warnings | M012 04JA59TNSJ |
| Diphenhydramine Hydrochloride | DIPHENHYDRAMINE HYDROCHLORIDE | A-S Medication Solutions | 5af966ae-535b-492b-ba2c-eeb4e40be959 | 2026-02-11 | Warnings, Adverse reactions | TC2D6JAD40 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.