Derma E Sun Protection Mineral
- Product NDC
- 54108-1486
- 11-digit product format
- 541081486
- Labeler code
- 54108
- Product ID
- 54108-1486_6b91329e-7dde-4226-8521-7f3c417a8b9e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc oxide
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- derma e
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-02-26
- Substance
- ZINC OXIDE
- Active strength
- 241 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Derma E Sun Protection Mineral
- Brand name suffix
- SPF 30
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 241 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SOI2LOH54Z |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 54108-1486-1 | Derma E Sun Protection Mineral SPF 30 | 1 in 1 BOX | POWDER | 1 | | 1 |
| 54108-1486-1 | Derma E Sun Protection Mineral SPF 30 | 5 g in 1 BOTTLE, WITH APPLICATOR | POWDER | 5 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54108-1486 | DERMA E SUN PROTECTION MINERAL SPF 30 (ZINC OXIDE) POWDER [DERMA E] | 1 | Current NDC, 2 package rows | 20240411_bb8e3df2-23e8-4ad0-a662-ff02d156e7b1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 54108-1486-1 | 54108148601 | 1 BOTTLE, WITH APPLICATOR in 1 BOX (54108-1486-1) / 5 g in 1 BOTTLE, WITH APPLICATOR | 2024-02-26 | No | No | Historical |