Daily Eclipse SPF 30 Tinted
- Product NDC
- 72492-000
- 11-digit product format
- 724920000
- Labeler code
- 72492
- Product ID
- 72492-000_9e3e3dbd-11ba-083c-e053-2a95a90a2e76
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Titanium Dioxide, Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- DermaMed Solutions, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-07-31
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE; TITANIUM DIOXIDE
- Active strength
- 6 g/50mL; g/50mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 72492-000-01 | 72492000001 | 50 mL in 1 BOTTLE, PUMP (72492-000-01) | 50 ml | 2018-07-31 | 0000-00-00 | No | No | Current |
| 72492-000-02 | 72492000002 | 118 mL in 1 BOTTLE, PUMP (72492-000-02) | 118 ml | 2018-07-31 | 0000-00-00 | No | No | Current |