NDC 72663-111-12 - Antiseptic
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
- 72663-111
- Requested NDC
- 72663-111-12
- Package NDCs from labels
- 72663-111-23, 72663-111-12
- Manufacturer
- Welly Health PCB
- Effective date
- 2025-01-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Antiseptic - Welly Health PCB | Welly Health PCB | 2025-01-29 | HUMAN OTC DRUG LABEL |
| Welly Human Repair Kit - Welly Health PBC | Welly Health PBC | 2021-12-31 | HUMAN OTC DRUG LABEL |
| Welly Quick Fix Kit - Welly Health PBC | Welly Health PBC | 2021-12-31 | HUMAN OTC DRUG LABEL |
| Welly Superhero Supplies Kit - Welly Health PBC | Welly Health PBC | 2021-12-31 | HUMAN OTC DRUG LABEL |
| Antiseptic - Welly Health PCB | Welly Health PCB | 2019-11-05 | HUMAN OTC DRUG LABEL |
| Welly Quick Fix Kit - Welly Health PBC | Welly Health PBC | 2019-03-14 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72663-111-23 | Antiseptic | 0.9 mL in 1 POUCH | GEL | 0.9 | 7 | |
| 72663-111-12 | Antiseptic | 12 in 1 BOX | GEL | 12 | 2 | |
| 72663-111-23 | Antiseptic | 0.9 mL in 1 POUCH | GEL | 0.9 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 72663-111 | ANTISEPTIC (ALCOHOL) GEL [WELLY HEALTH PCB] | 7 | Current NDC, Legacy NDC, 1 package rows | 20250130_85ce2c23-25d8-4b35-95ff-99f098d92bc9.zip |
| 72663-111 | ANTISEPTIC (ALCOHOL) GEL [WELLY HEALTH PCB] | 2 | Current NDC, Legacy NDC, 2 package rows | 20200207_515a2c1d-2c2c-4389-b042-0e880661db64.zip |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.