WOODSLEEP Sunscreen Balm
- Product NDC
- 85053-004
- 11-digit product format
- 850530004
- Labeler code
- 85053
- Product ID
- 85053-004_45cfc7ed-34a7-1f45-e063-6394a90a902b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TITANIUM DIOXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Shantou Woodsleep Biotechnology Co., Ltd.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-13
- Substance
- ARTEMISIA ARGYI LEAF
- Active strength
- .012 mg/60mg
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- WOODSLEEP Sunscreen Balm
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ARTEMISIA ARGYI LEAF | .012 mg/60mg |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2JYC99Q0WZ |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85053-004-01 | WOODSLEEP Sunscreen Balm | 60 mg in 1 BOTTLE, GLASS | CREAM | 60 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85053-004-01 | 85053000401 | 60 mg in 1 BOTTLE, GLASS (85053-004-01) | 60 mg | 2025-12-13 | No | No | Historical |