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 |
|---|---|---|---|---|---|---|
| ADVANCED REGULAR STRENGTH ANTACID | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE | WALGREEN COMPANY | 5faf6229-b0fd-58df-e053-2a91aa0ab3bb | 2025-10-30 | Warnings | M001 |
| GNP Hemorrhoidal | MINERAL OIL, PETROLATUM, PHENYLEPHRINE, HCL | Amerisource Bergen | b0f0ef97-9add-717f-e053-2a95a90a0eb0 | 2025-10-30 | Warnings | 04JA59TNSJ |
| Robitussin Maximum Strength Nighttime Cough DM | DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | Haleon US Holdings LLC | 44feee2f-25bc-48d4-8e13-db1d9daaaa90 | 2025-10-30 | Warnings | M012 |
| Robitussin Day and Night Cough Relief DM Max | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, DOXYLAMINE SUCCINATE | Haleon US Holdings LLC | b3d02c91-8f79-4eb4-a378-1072474c572c | 2025-10-30 | Warnings | M012 |
| Diphenhydramine HCl and Zinc Acetate | EXTRA STRENGTH ITCH RELIEF | HEB | 2aedbf1d-c8b7-4d5d-83ee-e38872c37d4f | 2025-10-30 | Warnings | TC2D6JAD40 |
| ROBITUSSIN MAXIMUM STRENGTH COUGH PLUS CHEST CONGESTION DM | DEXTROMETHORPHAN HBR, GUAIFENESIN | Haleon US Holdings LLC | f1d022dd-c2ca-497f-87d5-9ef3e20e8ea7 | 2025-10-30 | Warnings | M012 |
| Extra Strength Itch Relief | DIPHENHYDRAMINE HCL AND ZINC ACETATE | Meijer Distribution Inc | 02f9e270-6047-83b6-e063-6394a90afc27 | 2025-10-30 | Warnings | TC2D6JAD40 |
| Extra Strength Acetaminophen | ACETAMINOPHEN | NuCare Pharmaceuticals, Inc. | 41affa1a-5aac-7fc0-e063-6394a90a5557 | 2025-10-30 | Warnings | M013 362O9ITL9D |
| Endal | TRIPROLIDINE HCL, DEXTROMETHORPHAN HBR | Poly Pharmaceuticals, Inc. | fc5401e2-ed65-72e7-e053-6294a90a81f3 | 2025-10-30 | Warnings | M012 |
| Ibuprofen | IBUPROFEN | NuCare Pharmaceuticals,Inc. | f60445d3-807e-0bbf-e053-2995a90a1299 | 2025-10-30 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Diphenhydramine Hydrochloride | DIPHENHYDRAMINE HYDROCHLORIDE | Henry Schein, Inc. | af972e71-62ab-40c6-925a-cbcb4d6720a4 | 2025-10-30 | Warnings, Adverse reactions | TC2D6JAD40 |
| daytime | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Publix Super Markets Inc | c7cef266-46fc-49ab-a2e7-54fc56298659 | 2025-10-30 | Warnings | M012 04JA59TNSJ 362O9ITL9D |
| Regular Strength Antacid | CALCIUM CARBONATE | SAFEWAY | ce44254f-6e33-4cbd-a609-6a926376efaf | 2025-10-29 | Warnings | M001 H0G9379FGK |
| Extra Strength | CALCIUM CARBONATE | BETTER LIVING BRANDS, LLC | 9b311b76-1892-4b74-a07a-8b321436d4a0 | 2025-10-29 | Warnings | M001 H0G9379FGK |
| Extra Strength | ANTACID TABLETS | SAFEWAY | f91aa7da-8bdc-4fd2-a9de-fef21674e515 | 2025-10-29 | Warnings | M001 H0G9379FGK |
| Extra Strength Smooth | CALCIUM CARBONATE | SAFEWAY | 4314ac58-03aa-479c-a711-4818cc332531 | 2025-10-29 | Warnings | M001 H0G9379FGK |
| Extra Strength | ANTACID TABLETS | SAFEWAY | 5bdb868d-016d-4175-9283-86c5b77bb26e | 2025-10-29 | Warnings | M001 H0G9379FGK |
| Extra Strength | ANTACID TABLETS | SAFEWAY | 03853f03-081d-4a78-b383-66ac9754d46f | 2025-10-29 | Warnings | M001 H0G9379FGK |
| Allergy Relief | DIPHENHYDRAMINE HYDROCHLORIDE | SAM'S WEST INC | 16592ad7-b7cb-0837-e063-6394a90ae059 | 2025-10-29 | Warnings | M012 1049630 TC2D6JAD40 |
| Ultra Strength | CALCIUM CARBONATE | BETTER LIVING BRANDS LLC | 3ff92c9a-987f-468e-9e18-1e3e171ede14 | 2025-10-29 | Warnings | M001 H0G9379FGK |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.