sunscreen
- Product NDC
- 87357-001
- 11-digit product format
- 873570001
- Labeler code
- 87357
- Product ID
- 87357-001_48f13b1c-8105-881b-e063-6394a90a816d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TITANIUM DIOXIDE
- Dosage form
- LOTION
- Route
- CUTANEOUS
- Labeler
- Guangdong Zhoubang Biotechnology Co., Ltd
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-22
- Substance
- ETHYLHEXYL SALICYLATE; TITANIUM DIOXIDE
- Active strength
- 3; 2.85 g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- sunscreen
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ETHYLHEXYL SALICYLATE | 3 g/100mL |
| TITANIUM DIOXIDE | 2.85 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4X49Y0596W, 15FIX9V2JP |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87357-001-01 | sunscreen | 30 mL in 1 BOTTLE, GLASS | LOTION | 30 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87357-001-01 | 87357000101 | 30 mL in 1 BOTTLE, GLASS (87357-001-01) | 30 ml | 2026-01-22 | No | No | Current |