NDC 72663-746 - Welly Travel Medicine 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
- 72663-746
- Package NDCs from labels
- 72663-746-48
- Manufacturer
- Welly Health PBC
- Effective date
- 2020-04-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Welly Travel Medicine Kit - Welly Health PBC | Welly Health PBC | 2020-04-15 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72663-746-48 | Welly Travel Medicine Kit | 2 in 1 KIT | TABLET, CHEWABLE | 125 mg | 2 | |
| 72663-746-48 | Welly Travel Medicine Kit | 6 in 1 BLISTER PACK | TABLET, CHEWABLE | 12 | 125 mg | 2 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| Ibuprofen | IBUPROFEN CAPSULE | PUBLIX SUPER MARKETS INC | 10a6eba7-e400-ce97-e063-6294a90af3bd | 2026-06-23 | Warnings | WK2XYI10QM |
| IBUPROFEN | IBUPROFEN | DISCOUNT DRUG MART, INC. | d07ea9e3-88b0-4aa0-903a-10555dcca37d | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | DISCOUNT DRUG MART, INC. | aae40114-343e-12da-e053-2a95a90a9213 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | BJWC | 0ca0b6cf-7d1f-4673-b9b9-48f78d80c00a | 2026-06-23 | Warnings | WK2XYI10QM |
| pain relief | IBUPROFEN | Bionpharma Inc. | 2b4ecdd8-627a-445f-8ddc-f2b6c832c1e8 | 2026-06-23 | Warnings | WK2XYI10QM |
| dye-free pain relief | IBUPROFEN | Bionpharma Inc. | c46c9c36-8844-7b50-e053-2a95a90aa0e9 | 2026-06-23 | Warnings | WK2XYI10QM |
| dye-free pain relief | IBUPROFEN | Bionpharma Inc. | 4227d0b7-846a-dcb0-e063-6294a90af7d7 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | CHAIN DRUG MARKETING ASSOCIATION INC. | 3c1c1b65-f57f-62b0-e063-6294a90a1021 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Chain Drug Marketing Association, Inc. | 3802982a-2373-9ca3-e063-6394a90a0ab7 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | CHAIN DRUG MARKETING ASSOCIATION INC. | 4573753d-117b-a6f2-e063-6394a90ae2f9 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Chain Drug Marketing Association, Inc. | 3ed7faff-fd48-0a83-e063-6394a90aab14 | 2026-06-23 | Warnings | WK2XYI10QM |
| Pain Relief | IBUPROFEN | Albertsons Companies | f9deaeb7-efb3-4019-e053-6394a90a33d6 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | MEIJER DISTRIBUTION INC. | bc15fea8-0d86-4546-e053-2995a90abee3 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | MEIJER DISTRIBUTION INC. | a13ac87b-b395-685e-e053-2a95a90ab5d3 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Whole Foods Market, INC. | 32348505-744c-fbfd-e063-6394a90a82d7 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | AMERISOURCE BERGEN | 1afcf0c6-bd41-4621-9e44-d97b81221c12 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | AMERISOURCE BERGEN | a13cee82-1c4e-0cbe-e053-2a95a90a3ab8 | 2026-06-23 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | A-S Medication Solutions | 51de1183-d226-4869-a00a-f6c74e126a39 | 2026-06-23 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| DRAMAMINE CHEWABLE ORANGE | MECLIZINE HYDROCHLORIDE | Medtech Products Inc. | 30387e63-278d-412a-bcad-7965c7c0aea7 | 2026-06-23 | Warnings | HDP7W44CIO |
| Ibuprofen | IBUPROFEN | A-S Medication Solutions | 25a94943-9acc-49c8-a4da-7e07bb2c35eb | 2026-06-23 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.