Mineral SPF 30 Brush-On Sun Defense
- Product NDC
- 55789-1221
- 11-digit product format
- 557891221
- Labeler code
- 55789
- Product ID
- 55789-1221_4cf91c97-4f4b-4fe7-92d3-003bdff9242c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TITANIUM DIOXIDE and ZINC OXIDE
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Mineral Fusion brands
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-12-31
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE; TITANIUM DIOXIDE
- Active strength
- 200 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55789-1221-1 | Mineral SPF 30 Brush-On Sun Defense | 4 g in 1 TUBE, WITH APPLICATOR | POWDER | 4 | | 4 |
| 55789-1221-1 | Mineral SPF 30 Brush-On Sun Defense | 1 in 1 CARTON | POWDER | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55789-1221 | MINERAL SPF 30 BRUSH-ON SUN DEFENSE (TITANIUM DIOXIDE AND ZINC OXIDE) POWDER [MINERAL FUSION BRANDS] | 4 | Legacy NDC, 2 package rows | 20230208_0454007d-979f-4cc2-ae8d-7a2a11ca48dd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55789-1221-1 | 55789122101 | 1 TUBE, WITH APPLICATOR in 1 CARTON (55789-1221-1) > 4 g in 1 TUBE, WITH APPLICATOR | 2019-12-31 | 0000-00-00 | No | No | Current |