BODY / FACE SUNSCREEN SUN
- Product NDC
- 85897-374
- 11-digit product format
- 858970374
- Labeler code
- 85897
- Product ID
- 85897-374_4d372a4d-ba8f-b8e4-e063-6294a90ae9d8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BODY / FACE SUNSCREEN SUN
- Dosage form
- CREAM, AUGMENTED
- Route
- CUTANEOUS
- Labeler
- Guanghzou AiXin Biotech Co., Ltd
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2025-07-03
- Substance
- HOMOSALATE; OCTINOXATE
- Active strength
- 7.5; 7.5 g/1; g/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BODY / FACE SUNSCREEN SUN
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HOMOSALATE | 7.5 g/1 |
| OCTINOXATE | 7.5 g/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | V06SV4M95S, 4Y5P7MUD51 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85897-374-01 | BODY / FACE SUNSCREEN SUN | 5 in 1 BOX | CREAM, AUGMENTED | 5 | | 2 |
| 85897-374-01 | BODY / FACE SUNSCREEN SUN | 1 in 1 BAG | CREAM, AUGMENTED | 1 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85897-374-01 | 85897037401 | 5 BAG in 1 BOX (85897-374-01) / 1 CREAM, AUGMENTED in 1 BAG | 5 bag | 2025-07-08 | No | No | Current |