Umbrella Sunscreen
- Product NDC
- 35192-010
- 11-digit product format
- 351920010
- Labeler code
- 35192
- Product ID
- 35192-010_ef57d337-397b-1898-e053-2a95a90a4876
- 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
- 2012-06-01
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; TITANIUM DIOXIDE
- Active strength
- 9 g/113.4g; g/113.4g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 35192-010 | UMBRELLA SUNSCREEN (OCTINOXATE TITANIUM DIOXIDE) LOTION [CA-BOTANA INTERNATIONAL] | 18 | Legacy NDC | 20241211_5c6011ea-94e6-43e1-b00f-06cc2b402127.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 35192-010-02 | 35192001002 | 113.4 g in 1 TUBE (35192-010-02) | 113.4 g | 2017-11-09 | 0000-00-00 | No | No | Current |