Sunscreen
- Product NDC
- 35192-051
- 11-digit product format
- 351920051
- Labeler code
- 35192
- Product ID
- 35192-051_eecbb910-987b-f722-e053-2a95a90a8b13
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- EMULSION
- Route
- TOPICAL
- Labeler
- CA-Botana International
- Application
- M020
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2022-09-12
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 21 g/100g
- 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 |
|---|
| 35192-051 | SUNSCREEN (ZINC OXIDE) EMULSION [CA-BOTANA INTERNATIONAL] | 9 | Legacy NDC | 20250130_e74f7c79-59e2-f6e2-e053-2a95a90ad832.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 35192-051-01 | 35192005101 | 62.3 g in 1 PACKAGE (35192-051-01) | 62.3 g | 2022-09-30 | 0000-00-00 | No | No | Current |