Antioxidant Sunscreen SPF 40
- Product NDC
- 51326-829
- 11-digit product format
- 513260829
- Labeler code
- 51326
- Product ID
- 51326-829_1e23a07e-f101-477a-98ab-51df88e50464
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate and Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Topiderm, Inc.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2000-07-28
- Substance
- OCTINOXATE; ZINC OXIDE
- Active strength
- 75; 70 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Antioxidant Sunscreen SPF 40
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OCTINOXATE | 75 mg/mL |
| ZINC OXIDE | 70 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4Y5P7MUD51, SOI2LOH54Z |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51326-829-03 | Antioxidant Sunscreen SPF 40 | 105 mL in 1 BOTTLE, PLASTIC | LOTION | 105 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51326-829 | ANTIOXIDANT SUNSCREEN SPF 40 (OCTINOXATE AND ZINC OXIDE) LOTION [TOPIDERM, INC.] | 6 | Current NDC, Legacy NDC, 1 package rows | 20231109_2686378c-8827-47fb-b3ed-07438bd4e9e2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51326-829-03 | 51326082903 | 105 mL in 1 BOTTLE, PLASTIC (51326-829-03) | 105 ml | 2000-07-28 | 0000-00-00 | No | No | Current |