UV Capture Sun Pact
- Product NDC
- 58930-065
- 11-digit product format
- 589300065
- Labeler code
- 58930
- Product ID
- 58930-065_b9aa6a05-2925-464b-887f-01e4c7d6d027
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Titnium Dioxide, Ethylhexyl Methoxycinnamate, Octocrylene
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Carver Korea Co.,Ltd
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-07-01
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; OCTINOXATE; OCTOCRYLENE
- Active strength
- 1 g/10g; g/10g; g/10g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record