Bain de Soleil
- Product NDC
- 11523-7189
- 11-digit product format
- 115237189
- Labeler code
- 11523
- Product ID
- 11523-7189_eafff815-4099-d1c7-e053-2a95a90a3375
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Bayer HealthCare LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 1999-05-21
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE
- Active strength
- 25 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11523-7189-1 | 11523718901 | 1 TUBE in 1 CARTON (11523-7189-1) > 88 g in 1 TUBE | 1 tube | 1999-05-21 | 0000-00-00 | No | No | Current |