LBEL
- Product NDC
- 14783-013
- 11-digit product format
- 147830013
- Labeler code
- 14783
- Product ID
- 14783-013_40004acb-f09e-4a93-a249-c80242ed8804
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TITANIUM DIOXIDE, OXYBENZONE, ZINC OXIDE, and OCTINOXATE
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Ventura International, Limited
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-12-15
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; OXYBENZONE; ZINC OXIDE; OCTINOXATE
- Active strength
- 0 g/g; g/g; g/g; g/g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#