Antioxidant SPF
- Product NDC
- 85339-208
- 11-digit product format
- 853390208
- Labeler code
- 85339
- Product ID
- 85339-208_45b3a6e6-720c-2308-e063-6294a90ace4f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Teton Dermatology Holdings, Inc.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-10-27
- Substance
- ZINC OXIDE
- Active strength
- 160 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
- Antioxidant SPF
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 160 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 |
|---|
| 85339-208-50 | Antioxidant SPF | 50 g in 1 BOTTLE, PUMP | CREAM | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 85339-208 | ANTIOXIDANT SPF (ZINC OXIDE) CREAM [TETON DERMATOLOGY HOLDINGS, INC.] | 1 | Current NDC, 1 package rows | 20250515_3509a916-f3e1-9c53-e063-6394a90a5bff.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85339-208-50 | 85339020850 | 50 g in 1 BOTTLE, PUMP (85339-208-50) | 50 g | 2023-10-27 | No | No | Historical |