CLE CCC Deep
- Product NDC
- 69231-022
- 11-digit product format
- 692310022
- Labeler code
- 69231
- Product ID
- 69231-022_7af7b428-f4ce-9ce8-e053-2a91aa0af063
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Titanium Dioxide, Octinoxate, Octisalate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- KW ABSC, INC.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-11-18
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE
- Active strength
- 2 mg/30mL; mg/30mL; mg/30mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 69231-022-02 | 69231002202 | 1 CONTAINER in 1 PACKAGE (69231-022-02) > 30 mL in 1 CONTAINER (69231-022-01) | 1 container | 2018-11-18 | 0000-00-00 | No | No | Current |