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 |
|---|---|---|---|---|---|---|
| Allergy relief | LORATADINE | Bryant Ranch Prepack | e87aa69c-9ec6-482d-8e28-32542f6b9166 | 2025-02-04 | Warnings | 311372 7AJO3BO7QN |
| Ibuprofen | IBUPROFEN | NuCare Pharmaceuticals,Inc. | 0bee69ff-cf76-175e-e063-6294a90a42f6 | 2025-02-03 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| No Drip Nasal Mist | OXYMETAZOLINE SPRAY | CVS Health | f4b8ff54-47b5-4d18-bf4e-b101abb22a24 | 2025-02-03 | Warnings | M012 |
| Anti Diarrheal | LOPERAMIDE HCL | CHAIN DRUG MARKETING ASSOCIATION INC | 3d2d211f-546b-48fe-b47c-d4a254f952a3 | 2025-02-03 | Warnings | 978010 77TI35393C |
| Meclizine Hydrochloride | MECLIZINE HYDROCHLORIDE | Advanced Rx of Tennessee, LLC | 2d31ae73-3f09-a77c-e063-6294a90ade9a | 2025-02-02 | Warnings, Adverse reactions | 995666 HDP7W44CIO |
| WONDERBELLY MAXIMUM STRENGTH ANTACID | CALCIUM CARBONATE | Ginger Health Company | 2969ce5b-39ae-47b7-e063-6394a90a1909 | 2025-02-01 | Warnings | M001 H0G9379FGK |
| ALLERGY RELIEF | LORATADINE | TARGET CORPORATION | 7cb1364b-0852-3444-e053-2991aa0a3629 | 2025-02-01 | Warnings | 7AJO3BO7QN |
| Ibuprofen | IBUPROFEN | Bi-Mart | 7ceacd63-d5fa-4cab-b8f3-a5131c97bb90 | 2025-02-01 | Warnings | 310965 WK2XYI10QM |
| Diphenhydramine Hydrochloride | DIPHENHYDRAMINE HYDROCHLORIDE | Bryant Ranch Prepack | f40bfdfc-1cb4-4604-9790-fb8d1d5173c6 | 2025-01-31 | Warnings | M012 TC2D6JAD40 |
| TENSION HEADACHE RELIEF | ACETAMINOPHEN-CAFFEINE | TARGET CORPORATION | 8ed1679d-d3a1-11b1-e053-2995a90a61ad | 2025-01-31 | Warnings | M013 362O9ITL9D |
| ValuMeds Extra Strength Headache Relief | ACETAMINOPHEN, ASPIRIN, CAFFEINE | Cabinet Health P.B.C. | 0f864e73-e4b8-4e23-8990-8439ac17bd58 | 2025-01-31 | Warnings | M013 R16CO5Y76E 362O9ITL9D |
| Well at Walgreens | SODIUM BICARBONATE, SODIUM CHLORIDE | Walgreen Company | cb5d3d9d-2481-4303-b6af-0002de8c9065 | 2025-01-31 | Warnings | 8MDF5V39QO |
| Sinus Wash Packet | SODIUM BICARBONATE, SODIUM CHLORIDE | RITE AID CORPORATION | d5b44ae7-81e8-1413-e053-2995a90a5933 | 2025-01-31 | Warnings | 8MDF5V39QO |
| Sinus Wash Saline Refills Meijer | SODIUM BICARBONATE, SODIUM CHLORIDE | Meijer, Inc. | dd7465fe-503a-4e34-e053-2995a90a2778 | 2025-01-31 | Warnings | 8MDF5V39QO |
| SinuCleanse | SODIUM BICARBONATE, SODIUM CHLORIDE | ASCENT CONSUMER PRODUCTS, INC. | ff4df6c5-c85f-406a-89d7-8c2853fd5e10 | 2025-01-31 | Warnings | 8MDF5V39QO |
| CVS | SODIUM BICARBONATE, SODIUM CHLORIDE | CVS Pharmacy | bccefef8-f92d-42fc-90fc-86644d1df655 | 2025-01-31 | Warnings | 8MDF5V39QO |
| Well at Walgreens | SODIUM BICARBONATE, SODIUM CHLORIDE | Walgreen Company | bcd336b4-9189-44d5-ae6d-81e535eff6b5 | 2025-01-31 | Warnings | 8MDF5V39QO |
| SinuCleanse | SODIUM BICARBONATE, SODIUM CHLORIDE | ASCENT CONSUMER PRODUCTS, INC. | c33bf872-54aa-45e0-9e40-a6565a13f198 | 2025-01-31 | Warnings | 8MDF5V39QO |
| NIGHTIME COLD AND FLU | NIGHTIME COLD AND FLU | TARGET CORP | 9dee9b92-eac9-b07d-e053-2995a90a0602 | 2025-01-31 | Warnings | M012 362O9ITL9D |
| Rugby Chest Congestion Relief DM | DEXTROMETHORPHAN HYDROBROMIDE / GUAIFENESIN | Bryant Ranch Prepack | 7b23faa9-40c8-4cea-b9fb-487cce2664af | 2025-01-31 | Warnings | M012 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.