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 |
|---|---|---|---|---|---|---|
| Motion Sickness Relief | DIMENHYDRINATE | L.N.K. International, Inc. | 95aae32f-6b3f-469d-86a5-c201a53f862a | 2026-06-29 | Warnings | M009 |
| childrens allergy relief | LORATADINE | Kroger Company | 52934db1-b6fc-43ca-9a8c-66ff47a94745 | 2026-06-29 | Warnings | 7AJO3BO7QN |
| DAYTIME COLD AND FLU | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE | Meijer, Inc. | b3be2068-39e8-45f8-950e-afaee2c2520f | 2026-06-29 | Warnings | M012 362O9ITL9D |
| NIGHTTIME COUGH DM | DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 646f65f4-b9e4-4291-aadc-d2070848d35c | 2026-06-29 | Warnings | M012 |
| Acetaminophen PM | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | Chain Drug Marketing Association, Inc. | e58417f4-3575-4433-ac2e-b7bf9fe8ba10 | 2026-06-29 | Warnings | M013 TC2D6JAD40 362O9ITL9D |
| Sinus Pressure, Pain and Cough | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | DOLGENCORP, LLC | 259b6f12-50c0-4e7a-9a44-bdf7e9a20a56 | 2026-06-29 | Warnings | M012 04JA59TNSJ 362O9ITL9D |
| Diphenhydramine Hydrochloride | DIPHENHYDRAMINE HYDROCHLORIDE | Health Pharma USA LLC | 31755678-825c-b84a-e063-6294a90a5a83 | 2026-06-27 | Warnings | M012 1049630 TC2D6JAD40 |
| Dr Kids Pain and Fever | ACETAMINOPHEN | CalmCo LLC | 5534a784-a7b1-5599-e063-6294a90a7961 | 2026-06-27 | Warnings | M013 362O9ITL9D |
| TYLENOL Extra Strength | ACETAMINOPHEN | Select Consumer Group LLC | 529d3a51-a248-7c02-e063-6294a90a10ae | 2026-06-27 | Warnings | M013 362O9ITL9D |
| Diphenhydramine Hydrochloride | DIPHENHYDRAMINE HYDROCHLORIDE | Health Pharma USA LLC | 319e84fd-4033-f5eb-e063-6394a90aa2f3 | 2026-06-27 | Warnings | M012 1049630 TC2D6JAD40 |
| Stomach Relief Regular Strength | BISMUTH SUBSALICYLATE | Rugby Laboratories | 6166c04e-20c6-4678-b16d-517474445698 | 2026-06-26 | Warnings | M008 62TEY51RR1 |
| Ibuprofen | IBUPROFEN | HAWAII REPACK, INC. | 6239818c-747d-4cbb-9b41-27ca8bbce41b | 2026-06-26 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Sportpharm LLC | cef04ae4-e78a-454d-bb66-84b1d348c106 | 2026-06-26 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| HyVee Cough Drops Menthol | MENTHOL | HY-VEE, INC | 47a6f3c3-a6fa-dd61-e063-6394a90a4965 | 2026-06-26 | Warnings | M012 |
| HyVee Cough Drops Cherry | MENTHOL | HY-VEE, INC | 47a717e9-56b3-e771-e063-6394a90a5c17 | 2026-06-26 | Warnings | M012 |
| CalmCo Sleep Aid | DIPHENHYDRAMINE HCL | CalmCo LLC | 552d0e50-a58c-8e47-e063-6394a90a8f7b | 2026-06-26 | Warnings | TC2D6JAD40 |
| Ibuprofen mini dye free | IBUPROFEN | CHAIN DRUG MARKETING ASSOCIATION INC. | 552d9018-cc7e-7e1a-e063-6294a90a3322 | 2026-06-26 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | TOP CARE (Topco Associates LLC) | fb842f4d-1228-9a52-e053-6294a90adb41 | 2026-06-26 | Warnings | WK2XYI10QM |
| Calmco Allergy Relief | DIPHENHYDRAMINE HCL | CalmCo LLC | 5532fd37-cdd6-97ab-e063-6394a90a3c77 | 2026-06-26 | Warnings | M012 TC2D6JAD40 |
| Dr Kids Allergy Relief | DIPHENHYDRAMINE HCL | CalmCo LLC | 5533e705-b8d5-71cf-e063-6394a90a2010 | 2026-06-26 | Warnings | M012 TC2D6JAD40 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.