Purpose
- Product NDC
- 0187-5500
- 11-digit product format
- 001875500
- Labeler code
- 0187
- Product ID
- 0187-5500_25ecf41f-85d3-4f2b-9e4d-8ec40d6474d1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Octisalate and Oxybenzone
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Bausch Health US LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2013-10-07
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE; OXYBENZONE
- Active strength
- 76 mg/mL; mg/mL; mg/mL
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0187-5500-04 | 00187550004 | 1 BOTTLE, PUMP in 1 CARTON (0187-5500-04) > 118 mL in 1 BOTTLE, PUMP | 2013-10-07 | 0000-00-00 | No | No | Current |