Sunscreen
- Product NDC
- 35192-048
- 11-digit product format
- 351920048
- Labeler code
- 35192
- Product ID
- 35192-048_eee14030-3064-50a3-e053-2995a90a088c
- 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
- 2022-07-26
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 35192-048 | SUNSCREEN (ZINC OXIDE) EMULSION [CA-BOTANA INTERNATIONAL] | 6 | Legacy NDC | 20250420_e4ba1839-97d4-7952-e053-2a95a90a4df3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 35192-048-17 | 35192004817 | 61 g in 1 PACKAGE (35192-048-17) | 61 g | 2022-07-26 | 0000-00-00 | No | No | Current |