Face and Body Sunscreen
- Product NDC
- 87092-001
- 11-digit product format
- 870920001
- Labeler code
- 87092
- Product ID
- 87092-001_456f73af-cdd6-0080-e063-6394a90a77e8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Non-Nano Zinc Oxide 25%
- Dosage form
- CREAM
- Route
- CUTANEOUS
- Labeler
- Guangzhou Shengyanghui Industrial Trading Co., Ltd
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-09-16
- Substance
- ZINC OXIDE
- Active strength
- 25 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
- Face and Body Sunscreen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 25 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SOI2LOH54Z |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87092-001-01 | Face and Body Sunscreen | 1 g in 1 TUBE | CREAM | 1 | | 2 |
| 87092-001-02 | Face and Body Sunscreen | 1 in 1 BOX | CREAM | 1 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87092-001-01 | 87092000101 | 1 g in 1 TUBE | 1 g | | | | Historical |
| 87092-001-02 | 87092000102 | 1 TUBE in 1 BOX (87092-001-02) / 1 g in 1 TUBE (87092-001-01) | 1 tube | 2025-09-16 | No | No | Historical |