Sunscreen SPF50
- Product NDC
- 85769-478
- 11-digit product format
- 857690478
- Labeler code
- 85769
- Product ID
- 85769-478_45089529-5812-5968-e063-6294a90a2e24
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sunscreen SPF50
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Guangdong Xinjie Cosmetics Co.,Ltd.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-01
- Substance
- AVOBENZONE; OCTISALATE; OCTOCRYLENE
- Active strength
- 1; 1; 1 g/10g; g/10g; g/10g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85769-478-01 | Sunscreen SPF50 | 1 g in 1 BOTTLE | LOTION | 1 | | 1 |
| 85769-478-02 | Sunscreen SPF50 | 1 in 1 BOTTLE | LOTION | 1 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85769-478-01 | 85769047801 | 1 g in 1 BOTTLE | 1 g | | | | Historical |
| 85769-478-02 | 85769047802 | 1 BOTTLE in 1 BOTTLE (85769-478-02) / 1 g in 1 BOTTLE (85769-478-01) | 1 bottle | 2025-12-01 | No | No | Historical |