NDC 87625-113 - 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
- 87625-113
- 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 |
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 |
|---|---|---|---|---|---|---|
| Mucus DM | DEXTROMETHORPHAN HBR, GUAIFENESIN | Meijer Distribution, Inc. | 87cf4f25-b0e9-4f8b-bde3-0d0f26e2120e | 2026-03-06 | Warnings | M012 |
| Childrens Pain and Fever | ACETAMINOPHEN | Topco Associates, LLC | 87af092c-99e6-475d-81af-b9fd8fc337d7 | 2026-03-06 | Warnings | M013 362O9ITL9D |
| Aspirin Regular Strength | ASPIRIN | Rite Aid Corporation | 879e2258-f61b-47ad-a4b1-7d1e78823570 | 2026-03-05 | Warnings | M013 R16CO5Y76E |
| DIPHENHYDRAMINE | DIPHENHYDRAMINE HYDROCHLORIDE | Micro Labs Limited | a1110433-498a-48cb-ac79-5732fd4f8fba | 2026-03-05 | Warnings, Adverse reactions | TC2D6JAD40 |
| RYNEX PE | BROMPHENIRAMINE MALEATE AND PHENYLEPHRINE HCL | EDWARDS PHARMACEUTICALS, INC. | 77ae1cf6-b8e5-4f3c-b7bc-e2609a8991ef | 2026-03-05 | Warnings | M012 04JA59TNSJ |
| IBUPROFEN | IBUOROFEN | Direct_Rx | 90b8b80e-ab30-3590-e053-2a95a90a70ef | 2026-03-05 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Legacy Pharmaceutical Packaging, LLC | 5ca441f9-a4b4-4bd8-aa54-319fae4c3d1a | 2026-03-05 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Oxycodone/APAP | OXYCODONE/APAP | Direct_Rx | e84245ca-957f-e85b-e053-2a95a90a836b | 2026-03-05 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Ibuprofen | IBUPROFEN | Direct_Rx | 1aa11b52-1aca-9219-e063-6294a90a470f | 2026-03-05 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Loratadine | LORATADINE | NuCare Pharmaceuticals,Inc. | c0e3057d-2dd2-de2b-e053-2995a90a1a1d | 2026-03-05 | Warnings | 311372 7AJO3BO7QN |
| Childrens Cold and Allergy | BROMPHENIRAMINE MALEATE, PHENYLEPHRINE HCL | Best Choice (Valu Merchandisers Company) | 042f9449-4af0-4b15-bb3e-236afeb1e11f | 2026-03-05 | Warnings | M012 04JA59TNSJ |
| Sleep Aid | DIPHENHYDRAMINE HCL | Wal-Mart Stores Inc | 5ef35ab9-b6e8-4c88-a623-35ac9d6bd359 | 2026-03-05 | Warnings | TC2D6JAD40 |
| Aspirin | ASPIRIN | ARMY AND AIR FORCE EXCHANGE SERVICE | 87c580d3-6009-4be9-aea7-13539fbe6e31 | 2026-03-05 | Warnings | M013 212033 R16CO5Y76E |
| Mucus Relief | GUAIFENESIN | Amerisource Bergen | 087a3a0b-8d3f-45ed-8807-0af47b446cac | 2026-03-05 | Warnings | M012 |
| Mucus Relief DM | DEXTROMETHORPHAN HBR 20MG GUAIFENESIN 400MG | NUVICARE LLC | 6c4bc7d1-09d9-4311-8457-a1d47ab02a5a | 2026-03-05 | Warnings | M012 |
| Aspirin Low Dose Chewable Orange | ASPIRIN | MAJOR PHARMACEUTICALS | fb3a8e38-e991-49c9-93dc-1d29c0a97ba3 | 2026-03-05 | Warnings | M013 R16CO5Y76E |
| Allergy Relief childrens | DIPHENHYDRAMINE HCL | WALMART INC. | dceb99a9-4aa3-4acc-b632-9a4ba8c87919 | 2026-03-04 | Warnings | M012 TC2D6JAD40 |
| AMAZON Childrens Multi Symptom Cold | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | AMAZON.COM SERVICES LLC | 26101105-a6cf-4b51-a639-9d078542fea3 | 2026-03-04 | Warnings | M012 04JA59TNSJ |
| Allergy Relief Childrens | DIPHENHYDRAMINE HCL | Major Pharmaceuticals | 3a976e90-c6af-4414-984e-9987158c9e98 | 2026-03-04 | Warnings | M012 TC2D6JAD40 |
| Ibuprofen Minis | IBUPROFEN | Grocery Outlet, Inc. | 44665e3d-37a7-a1a7-e063-6294a90ab376 | 2026-03-04 | Warnings | WK2XYI10QM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.