HANCHOBIT Sunscreen
- Product NDC
- 85164-005
- 11-digit product format
- 851640005
- Labeler code
- 85164
- Product ID
- 85164-005_449ff8f8-fe08-7bce-e063-6394a90ace56
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TITANIUM DIOXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- HANCHOYEANBIOTEC Co.,Ltd.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-11-07
- Substance
- BETULA ALBA JUICE
- Active strength
- .01 mg/50mg
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- HANCHOBIT Sunscreen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BETULA ALBA JUICE | .01 mg/50mg |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9G931M6I4G |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85164-005-01 | HANCHOBIT Sunscreen | 50 mg in 1 BOTTLE, PLASTIC | CREAM | 50 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85164-005-01 | 85164000501 | 50 mg in 1 BOTTLE, PLASTIC (85164-005-01) | 50 mg | 2025-11-07 | No | No | Current |