GLOW Tinted Mineral Sunscreen
- Product NDC
- 85386-204
- 11-digit product format
- 853860204
- Labeler code
- 85386
- Product ID
- 85386-204_4604b00d-be67-15a2-e063-6294a90afce4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Allure Esthetics
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-08-02
- Substance
- ZINC OXIDE
- Active strength
- 200 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- GLOW Tinted Mineral Sunscreen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 200 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SOI2LOH54Z |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85386-204-60 | GLOW Tinted Mineral Sunscreen | 60 g in 1 BOTTLE, PUMP | CREAM | 60 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85386-204-60 | 85386020460 | 60 g in 1 BOTTLE, PUMP (85386-204-60) | 60 g | 2022-08-02 | No | No | Current |