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 |
|---|---|---|---|---|---|---|
| ACTINEL PEDIATRIC | DEXTROMETHORPHAN HBR,GUAIFENESIN,PSEUDOEPHEDRINE HCL | ACTIPHARMA, LLC | 6bb92d74-4893-40b8-af58-eb307155e876 | 2025-07-08 | Warnings | M012 |
| topcare pain relief | ACETAMINOPHEN | Topco Associates LLC | 6aca88df-d3b5-4a60-b23b-1e66dc41ee7b | 2025-07-08 | Warnings | M013 362O9ITL9D |
| Nighttime Cold and Flu Maximum Strength | ACETAMINOPHEN, DIPHENHYDRAMINE HCI, PHENYLEPHRINE HCI | Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) | 776b7c67-56c7-420c-82b2-9a176d998396 | 2025-07-08 | Warnings | M012 04JA59TNSJ TC2D6JAD40 362O9ITL9D |
| ACTICON | DEXBROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE | ACTIPHARMA, LLC | 847014ab-86ae-40c5-8e7f-f1ddea14f1b3 | 2025-07-08 | Warnings | M012 |
| Hydrocodone Bitartrate and Acetaminophen | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | Genus Lifesciences Inc. | a9fb9779-76a5-407a-a155-84f198004ae2 | 2025-07-08 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| equate childrens pain and fever | ACETAMINOPHEN | Wal-Mart Stores Inc | f15037a5-4e43-4dd6-93b8-b37a1cc22cd6 | 2025-07-07 | Warnings | M013 362O9ITL9D |
| Dual Action Complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | Kroger Company | bf2fcb88-418f-4d5d-85ba-ec165a53ab04 | 2025-07-07 | Warnings | H0G9379FGK |
| Mucus Relief | GUAIFENESIN 400 MG | Cabinet Health, Inc. | 26a51b0e-039c-663c-e063-6394a90ad384 | 2025-07-07 | Warnings | M012 |
| MGC Health Antacid Soft Chews Cherry Flavor | CALCIUM CARBONATE | Xiamen Kang Zhongyuan Biotechnology Co., Ltd. | 3958ec0a-8f32-6918-e063-6294a90ac1c4 | 2025-07-07 | Warnings | M001 H0G9379FGK |
| Sodium Citrate and Citric Acid | SODIUM CITRATE AND CITRIC ACID MONOHYDRATE | Belleview Biosciences LLC | 3245e0e5-5e7f-c3f7-e063-6394a90ac258 | 2025-07-07 | Adverse reactions | XF417D3PSL |
| Ibuprofen | IBUPROFEN | Sun Pharmaceutical Industries, Inc. | 6cf3328b-da8f-4f6b-8237-16a4d6b9c833 | 2025-07-07 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Sun Pharmaceutical Industries, Inc. | f4dad3d6-1366-4bdf-99eb-370ab74a6b9e | 2025-07-07 | Warnings | WK2XYI10QM |
| EZ Nite Sleep | DIPHENHYDRAMINE HCL | Safeway, Inc. | 21a68c60-3005-43bb-8ec5-7982239c93f8 | 2025-07-07 | Warnings | M012 TC2D6JAD40 |
| Equate Acid Reducer Complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | Wal-Mart Stores Inc | cb683c1c-db81-40a9-9ec5-f8dfa0dcf812 | 2025-07-07 | Warnings | H0G9379FGK |
| dg health dual back pain reliever | ACETAMINOPHEN, IBUPROFEN | Dolgencorp Inc | b52cfead-1cff-4e11-9953-f470fb785c73 | 2025-07-07 | Warnings | WK2XYI10QM 362O9ITL9D |
| Aluminum Hydroxide, Magnesium Hydroxide, and Simethicone | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND SIMETHICONE | Major Pharmaceuticals | 1bc90fa7-fcce-4a9b-862f-f30ab602ecab | 2025-07-07 | Warnings | M001 |
| Dual Action Complete | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | H E B | ea712fc4-7f27-4556-b1b8-028f3f6ce57a | 2025-07-07 | Warnings | H0G9379FGK |
| DG Health acid reducer complete | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Dolgencorp, LLC | 95c2c515-0f31-49d9-b799-7aaded81a37c | 2025-07-07 | Warnings | H0G9379FGK |
| Childrens Acetaminophen Oral Liquid Grape Flavor | ACETAMINOPHEN | AARNA USA INC. | 39347f5d-2d3c-0c23-e063-6294a90a3a46 | 2025-07-05 | Warnings | M013 362O9ITL9D |
| MUCUS RELIEF | GUAIFENESIN 400 MG | Pioneer Life Sciences, LLC | 8188b66a-5405-4e62-bde6-63ebc1f22b16 | 2025-07-04 | Warnings | M012 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.