ULTRA SILK PROTECTION SUNSCREEN
- Product NDC
- 85564-208
- 11-digit product format
- 855640208
- Labeler code
- 85564
- Product ID
- 85564-208_4627b917-42b2-f065-e063-6394a90adeae
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- SKINFINITY
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-04-20
- Substance
- ZINC OXIDE
- Active strength
- 160 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
- ULTRA SILK PROTECTION SUNSCREEN
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 160 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 |
|---|
| 85564-208-50 | ULTRA SILK PROTECTION SUNSCREEN | 50 g in 1 BOTTLE, PUMP | CREAM | 50 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85564-208-50 | 85564020850 | 50 g in 1 BOTTLE, PUMP (85564-208-50) | 50 g | 2022-04-20 | No | No | Current |