ULTRA UMBRELLA
- Product NDC
- 35192-011
- 11-digit product format
- 351920011
- Labeler code
- 35192
- Product ID
- 35192-011_ef69b9bd-79ba-ca94-e053-2a95a90a5e56
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE TITANIUM DIOXIDE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- CA-BOTANA INTERNATIONAL
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-08-01
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; TITANIUM DIOXIDE
- Active strength
- 5 g/113.4g; g/113.4g
- 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 product | product | 35192-011 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 35192-011 | 35192-011-02 | D | Discontinued by firm | 2026-10-05 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 35192-011-02 | 35192001102 | 113.4 g in 1 TUBE (35192-011-02) | 113.4 g | 2013-08-01 | 0000-00-00 | No | No | Current |