OPEN NATURE SPF 50 MINERAL SUNSCREEN
- Product NDC
- 21130-723
- 11-digit product format
- 211300723
- Labeler code
- 21130
- Product ID
- 21130-723_24770eab-d19c-679d-e063-6394a90a74a2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC OXIDE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- SAFEWAY, INC.
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-12-05
- Substance
- ZINC OXIDE
- Active strength
- 216 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
- OPEN NATURE SPF 50 MINERAL SUNSCREEN
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 216 mg/mL |
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 |
|---|
| 21130-723-03 | OPEN NATURE SPF 50 MINERAL SUNSCREEN | 89 mL in 1 TUBE | LOTION | 89 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21130-723 | OPEN NATURE SPF 50 MINERAL SUNSCREEN (ZINC OXIDE) LOTION [SAFEWAY, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241016_a6020d2f-55c4-adfc-e053-2a95a90ad238.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 21130-723-03 | 21130072303 | 89 mL in 1 TUBE (21130-723-03) | 89 ml | 2018-12-05 | 0000-00-00 | No | No | Current |