Octinoxate, Octisalate, Avobenzone
- Product NDC
- 41250-863
- 11-digit product format
- 412500863
- Labeler code
- 41250
- Product ID
- 41250-863_b42ca293-2c19-4d09-b67c-6c32bc3208f4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Octisalate, Avobenzone
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Meijer Distribution, Inc
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-02-25
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; OCTINOXATE; OCTISALATE
- Active strength
- 31 mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 41250-863-26 | 41250086326 | 118 mL in 1 BOTTLE, PLASTIC (41250-863-26) | 118 ml | 2016-02-25 | 0000-00-00 | No | No | Current |