YONHISDAT Sunscreen Powder
- Product NDC
- 85950-002
- 11-digit product format
- 859500002
- Labeler code
- 85950
- Product ID
- 85950-002_3b511159-bd76-93c3-e063-6394a90a3113
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- titanium dioxide, zinc oxide powder
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- PANERGYTEK USA INC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-07-27
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 19.5; 24 g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- YONHISDAT Sunscreen Powder
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TITANIUM DIOXIDE | 19.5 g/100g |
| ZINC OXIDE | 24 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 15FIX9V2JP, SOI2LOH54Z |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85950-002-01 | YONHISDAT Sunscreen Powder | 5 g in 1 BOTTLE | POWDER | 5 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85950-002-01 | 85950000201 | 5 g in 1 BOTTLE (85950-002-01) | 5 g | 2025-07-27 | No | No | Historical |