BISUTANG Sunscreen
- Product NDC
- 84753-034
- 11-digit product format
- 847530034
- Labeler code
- 84753
- Product ID
- 84753-034_37fdb01b-929f-6a60-e063-6394a90a94e0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BISUTANG Sunscreen
- Dosage form
- LIQUID
- Route
- CUTANEOUS
- Labeler
- Guangdong Bisutang Biotechnology Co Ltd
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-20
- Substance
- TITANIUM DIOXIDE
- Active strength
- 3 g/3g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BISUTANG Sunscreen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TITANIUM DIOXIDE | 3 g/3g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 15FIX9V2JP |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84753-034-01 | BISUTANG Sunscreen | 30 g in 1 BOTTLE, PLASTIC | LIQUID | 30 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84753-034-01 | 84753003401 | 30 g in 1 BOTTLE, PLASTIC (84753-034-01) | 30 g | 2025-06-20 | No | No | Current |