LBEL
- Product NDC
- 14783-059
- 11-digit product format
- 147830059
- Labeler code
- 14783
- Product ID
- 14783-059_1865a6da-ed21-4419-82a8-f94342252275
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Titanium Dioxide, Zinc Oxide, and Octinoxate
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Ventura International LTD.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2013-05-27
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE; OCTINOXATE
- Active strength
- 0 g/g; g/g; g/g
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#