OUHOE Face Body Sunscreen
- Product NDC
- 85163-017
- 11-digit product format
- 851630017
- Labeler code
- 85163
- Product ID
- 85163-017_46d36f60-2a5e-816e-e063-6294a90a2ddc
- 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
- 2025-12-26
- Substance
- BEESWAX; BUTYROSPERMUM PARKII (SHEA) BUTTER; OLEA EUROPAEA (OLIVE) FRUIT OIL; PROPOLIS WAX; SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL
- Active strength
- .016; .016; .016; .016; .016 mg/80mg; mg/80mg; mg/80mg; mg/80mg; mg/80mg
- Pharmacologic classes
- Lipid Emulsion [EPC], Lipids [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- OUHOE Face Body Sunscreen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BEESWAX | .016 mg/80mg |
| BUTYROSPERMUM PARKII (SHEA) BUTTER | .016 mg/80mg |
| OLEA EUROPAEA (OLIVE) FRUIT OIL | .016 mg/80mg |
| PROPOLIS WAX | .016 mg/80mg |
| SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL | .016 mg/80mg |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2ZA36H0S2V, K49155WL9Y, 6UYK2W1W1E, 6Y8XYV2NOF, 724GKU717M |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85163-017-01 | OUHOE Face Body Sunscreen | 80 mg in 1 BOTTLE, PLASTIC | CREAM | 80 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85163-017-01 | 85163001701 | 80 mg in 1 BOTTLE, PLASTIC (85163-017-01) | 80 mg | 2025-12-26 | No | No | Historical |