Sunscreen
- Product NDC
- 35192-050
- Requested package NDC
- 35192-050-17
- 11-digit product format
- 351920050
- Labeler code
- 35192
- Product ID
- 35192-050_eee0b691-8f1a-8128-e053-2a95a90a3969
- 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
- 2022-07-31
- 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
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 35192-050 | 35192-050-17 | D | Discontinued by firm | 2026-10-12 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 35192-050-17 | 35192005017 | 61 g in 1 PACKAGE (35192-050-17) | 61 g | 2022-07-31 | 0000-00-00 | No | No | Current |