OUHOE Sunscreen
- Product NDC
- 85163-010
- 11-digit product format
- 851630010
- Labeler code
- 85163
- Product ID
- 85163-010_448dfe7f-aab7-9159-e063-6294a90a8fe9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TITANIUM DIOXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Shantou Ouhoe Technology Co., Ltd.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-11-07
- Substance
- CENTELLA ASIATICA LEAF; GLYCYRRHIZA URALENSIS ROOT
- Active strength
- .01; .01 mg/50mg; 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
- OUHOE Sunscreen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CENTELLA ASIATICA LEAF | .01 mg/50mg |
| GLYCYRRHIZA URALENSIS ROOT | .01 mg/50mg |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6810070TYD, 42B5YD8F0K |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85163-010-01 | OUHOE 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 |
|---|
| 85163-010-01 | 85163001001 | 50 mg in 1 BOTTLE, PLASTIC (85163-010-01) | 50 mg | 2025-11-07 | No | No | Historical |