LBEL
- Product NDC
- 14783-011
- 11-digit product format
- 147830011
- Labeler code
- 14783
- Product ID
- 14783-011_c3d86ea0-9722-4082-9fdf-2d3ac62b60f3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE, OXYBENZONE, and TITANIUM DIOXIDE
- Dosage form
- LIPSTICK
- 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
- OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE
- Active strength
- 0 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#