NDC 87625-104 - 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
- 87625-104
- 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 |
|---|---|---|---|---|---|---|
| HyVee Cough Drops Honey Lemon | MENTHOL | Xiamen Kang Zhongyuan Biotechnology Co., Ltd. | fae96736-1453-42fe-8158-cde770b23165 | 2026-01-02 | Warnings | M012 |
| HyVee Cough Drops Menthol | MENTHOL | Xiamen Kang Zhongyuan Biotechnology Co., Ltd. | 8cac1229-8e8e-4d8c-9f18-c2cd0f6f50bd | 2026-01-02 | Warnings | M012 |
| Ibuprofen | IBUPROFEN | Northwind Health Company, LLC | 2f12a20c-4293-d18a-e063-6294a90a3afc | 2026-01-02 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Reliable-1 Tussin | GUAIFENESIN | RELIABLE 1 LABORATORIES LLC | 2a33ff82-49df-7aaa-e063-6294a90a1281 | 2026-01-02 | Warnings | M012 |
| Tussin DMMax | DEXTROMETHORPHAN HBR, GUAIFENESIN | RELIABLE 1 LABORATORIES LLC | c4bb2e12-e0f6-4cbf-ad24-cfad9326f7fa | 2026-01-02 | Warnings | M012 |
| Pain Relief Extra Strength, Non-Aspirin | ACETAMINOPHEN | CHAIN DRUG MARKETING ASSOCIATION INC | 1fb5e871-45fd-46fe-bf73-5192f8316e8e | 2026-01-02 | Warnings | M013 362O9ITL9D |
| Severe Sinus Pain and Congestion Daytime | ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL | CVS Pharmacy | 4af347ce-9745-4a5e-8ce9-e7c97a0a6cc7 | 2026-01-02 | Warnings | M012 04JA59TNSJ 362O9ITL9D |
| Pain Reliever Extra Strength | ACETAMINOPHEN | Valu Merchandisers Company | 0005aafa-08f8-4990-a54d-cc097195708f | 2026-01-02 | Warnings | M013 362O9ITL9D |
| IBUPROFEN PM | DIPHENHYDRAMINE CITRATE, IBUPROFEN | Safeway | 57e8f0d7-1f21-4fda-8b21-3caa54fae4e6 | 2026-01-02 | Warnings | WK2XYI10QM |
| Extra Strength Pain Reliever | ACETAMINOPHEN | Walmart Inc. | 152bb455-da5b-ae13-e063-6394a90acab0 | 2026-01-01 | Warnings | M013 362O9ITL9D |
| Dr. Cocoa for Children Pain and Fever | ACETAMINOPHEN | Infirst Healthcare Inc. | 486ea294-6d18-a907-e063-6294a90ad284 | 2026-01-01 | Warnings | M013 362O9ITL9D |
| Meclizine Hydrochloride | MECLIZINE HYDROCHLORIDE | Northwind Health Company, LLC | f2b4716c-411a-62cd-e053-2a95a90a6f4b | 2026-01-01 | Warnings, Adverse reactions | 995666 HDP7W44CIO |
| Ibuprofen | IBUPROFEN | Northwind Health Company, LLC | c20f1f4d-59b3-6bbe-e053-2a95a90abaf1 | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Northwind Health Company, LLC | ab313564-27dc-0297-e053-2a95a90a6690 | 2026-01-01 | Warnings | 310965 WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Northwind Health Company, LLC | dac07d8f-6b6f-20ab-e053-2a95a90af3ba | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Good Sense anti diarrheal | LOPERAMIDE HYDROCHLORIDE | Northwind Health Company, LLC | db47cc0a-e301-0310-e053-2a95a90a7f5d | 2026-01-01 | Warnings | 978010 77TI35393C |
| Ibuprofen | IBUPROFEN | Northwind Health Company, LLC | da6c72ad-009f-3d7f-e053-2995a90a68e9 | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| ibuprofen | IBUPROFEN | Northwind Health Company, LLC | da6c2802-5d15-dbcb-e053-2a95a90a2561 | 2026-01-01 | Warnings | 310965 WK2XYI10QM |
| Motrin IB | IBUPROFEN | Savings Distributors LLC | 56846774-8413-c306-e063-6394a90a2be8 | 2026-01-01 | Warnings | 310965 WK2XYI10QM |
| NUVALU VAPORIZING CHEST RUB | CAMPHOR, EUCALYPTUS OIL, MENTHOL | JC SALES | 490b2d1e-3a1d-1a52-e063-6394a90a00ba | 2026-01-01 | Warnings | M012 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.