FEVANZON Isolation Sunscreen
- Product NDC
- 80815-003
- 11-digit product format
- 808150003
- Labeler code
- 80815
- Product ID
- 80815-003_3e258263-0b73-4301-bff8-a8879aa17c1d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone,homosalate,Octisalate,Oxybenzone
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- HBB INTERNATIONAL INC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-08-22
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
- Active strength
- 3 g/100mL; g/100mL; g/100mL; g/100mL; mg/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80815-003-01 | 80815000301 | 50 BOTTLE in 1 CARTON (80815-003-01) > 50 mL in 1 BOTTLE | 50 bottle | 2020-08-22 | 0000-00-00 | No | No | Current |