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 |
|---|---|---|---|---|---|---|
| Nasal Four | PHENYLEPHRINE HYDROCHLORIDE | HyVee Inc | 19879fc8-4962-4c6e-87ed-b874d1d564af | 2026-04-01 | Warnings | M012 04JA59TNSJ |
| Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Lidl US LLC | 7227b330-590b-4731-8a58-e05a0233dd8a | 2026-04-01 | Warnings | M012 04JA59TNSJ 362O9ITL9D |
| SudoGest | CHLORPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HCL | Major Pharmaceuticals | 7cd8f7f3-c262-4f7c-bcaf-068be2c952f9 | 2026-04-01 | Warnings | M012 |
| menstrual pain relief maximum strength | ACETAMINOPHEN, PAMABROM, PYRILAMINE MALEATE | Rite Aid Corporation | 4a4ce4cd-1554-4772-a6f4-8f7830544949 | 2026-04-01 | Warnings | 362O9ITL9D |
| Sanatos Daytime Relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Pharmadel LLC | 4c26be18-733a-e4a8-e063-6294a90a8b02 | 2026-04-01 | Warnings | M012 04JA59TNSJ 362O9ITL9D |
| Sanatos Nighttime Relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE | Pharmadel LLC | 4c26c8bf-0143-ddca-e063-6294a90a3552 | 2026-04-01 | Warnings | M012 362O9ITL9D |
| Itch Relief | DIPHENHYDRAMINE HCL AND ZINC ACETATE | CVS Pharmacy | 7e921988-ec66-38dc-e053-2a91aa0a7346 | 2026-04-01 | Warnings | TC2D6JAD40 |
| ALLERGY RELIEF 10 mg | LORATADINE | TWIN MED LLC | d943f548-aa0d-4476-e053-2a95a90a7bd4 | 2026-04-01 | Warnings | 311372 7AJO3BO7QN |
| Codeine-Guaifenesin | CODEINE PHOSPHATE AND GUAIFENESIN | Method Pharmaceuticals, LLC | fe126254-6ee6-48c3-965c-96e4276a5314 | 2026-04-01 | Warnings | M012 |
| Walgreens Pain Relief with Lidocaine | LIDOCAINE, PHENYLEPHRINE HCL | Walgreens Co | 3ce78f2f-0264-f406-e063-6294a90a7e03 | 2026-04-01 | Warnings | 04JA59TNSJ |
| TUMS Smoothies | CALCIUM CARBONATE | Haleon US Holdings LLC | c22944b8-8733-4689-be0c-f320467f79ea | 2026-04-01 | Warnings | M001 H0G9379FGK |
| Wispirin | ASPIRIN | Wisdrug AG | 4e70ec5e-d033-a525-e063-6394a90a5a93 | 2026-04-01 | Warnings | M013 R16CO5Y76E |
| Ibuprofen Dye-Free | IBUPROFEN | Wal-Mart Stores Inc | 23cb5001-6aeb-434a-b2e8-aaf8bbab9dc6 | 2026-04-01 | Warnings | 310965 WK2XYI10QM |
| Nighttime Sleep Aid | DIPHENHYDRAMINE HCL | United Natural Foods, Inc. dba UNFI | 6c9b7576-428a-4884-8331-bb312c9046bd | 2026-04-01 | Warnings | 1049630 TC2D6JAD40 |
| Meclizine HCL 12.5 mg | MECLIZINE HCL 12.5 MG | Proficient Rx LP | 3ffa63f2-ea06-4be0-9f59-162c2a9604fc | 2026-04-01 | Warnings | M009 HDP7W44CIO |
| Omeprazole/Bicarbonate | OMEPRAZOLE AND SODIUM BICARBONATE | Proficient Rx LP | 4d642036-7175-4f29-9f07-dbd282231d4a | 2026-04-01 | Warnings, Adverse reactions | 8MDF5V39QO |
| Care One Ibuprofen PM | DIPHENHYDRAMINE CITRATE AND IBUPROFEN | American Sales Company | d5bf76d1-6fed-4f6b-8507-3e8973295d67 | 2026-04-01 | Warnings | WK2XYI10QM |
| Good Neighbor Pharmacy Mucus Relief | GUAIFENESIN | AmerisourceBergen Drug Corp | 200dddd9-e3ff-4cec-a164-d1c9a698f121 | 2026-03-31 | Warnings | M012 |
| Aspirin Regimen | ASPIRIN | Cardinal Health 110, LLC. DBA Leader | ef2d75ee-9ed7-4b53-adbc-2ec40364da63 | 2026-03-31 | Warnings | M013 R16CO5Y76E |
| ALLERGY RELIEF | LORATADINE | CARDINAL HEALTH 110, LLC. DBA LEADER | 052e0ea2-441f-42cc-b62c-f2574f995bff | 2026-03-31 | Warnings | 7AJO3BO7QN |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.