Vichy Laboratoires Capital Soleil SPF 50 Ultra Light Sunscreen
- Product NDC
- 49967-891
- 11-digit product format
- 499670891
- Labeler code
- 49967
- Product ID
- 49967-891_a2ee73c2-2965-49c5-b5f8-bf120922a0d9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene and Oxybenzone
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- L'Oreal USA Products Inc
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2011-07-01
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
- Active strength
- 30 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record