LBEL Clarite Clarifying Effect Foundation SPF 30
- Product NDC
- 14783-221
- 11-digit product format
- 147830221
- Labeler code
- 14783
- Product ID
- 14783-221_4a1f8fe0-9497-481f-aca7-dc023f67b28b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate and Zinc Oxide
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Ventura International LTD
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-12-26
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; ZINC OXIDE
- Active strength
- 0 g/g; g/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 14783-221-02 | 14783022102 | 1 CONTAINER in 1 BOX (14783-221-02) > 9 g in 1 CONTAINER (14783-221-01) | 1 container | 2018-12-26 | 0000-00-00 | No | No | Current |