NDC 72249-001 - Dandrene
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
- 72249-001
- Package NDCs from labels
- 72249-001-01
- Manufacturer
- Divine Skin Laboratories S.A. de C.V. | A.I.G. Technologies, Inc.
- Effective date
- 2020-11-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dandrene Conditioner | Divine Skin Laboratories S.A. de C.V. | A.I.G. Technologies, Inc. | 2020-11-30 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72249-001-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-6635-a426-e053-dadaa90af4c2 | Dandrene Conditioner |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72249-001-01 | Dandrene | 1 in 1 BOX | LOTION | 1 | 2 | |
| 72249-001-01 | Dandrene | 205 g in 1 BOTTLE | LOTION | 205 | 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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.