Mineral Sunscreen
- Product NDC
- 35192-044
- 11-digit product format
- 351920044
- Labeler code
- 35192
- Product ID
- 35192-044_efe3cf8f-38f5-3840-e053-2a95a90a8363
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- EMULSION
- Route
- TOPICAL
- Labeler
- CA-Botana International
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-08-15
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 13 g/12.81g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 35192-044-15 | Mineral Sunscreen | 61 g in 1 TUBE | EMULSION | 61 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 35192-044 | MINERAL SUNSCREEN (ZINC OXIDE) EMULSION [CA-BOTANA INTERNATIONAL] | 6 | Legacy NDC, 1 package rows | 20241215_28e0ab0f-ab45-d61a-e063-6294a90ac4fc.zip |
| 35192-044 | MINERAL SUNSCREEN (ZINC OXIDE) EMULSION [CA-BOTANA INTERNATIONAL] | 5 | Legacy NDC | 20250101_c7929b18-76f5-af11-e053-2a95a90a183c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 35192-044-01 | 35192004401 | 61 g in 1 TUBE (35192-044-01) | 61 g | 2021-08-15 | 0000-00-00 | No | No | Current |
| 35192-044-15 | 35192004415 | 61 g in 1 TUBE | 61 g | | | | | Historical |