Dr.Jart Every Sun Day Mineral Sun Screen
- Product NDC
- 49404-143
- 11-digit product format
- 494040143
- Labeler code
- 49404
- Product ID
- 49404-143_f05dcd4e-dea8-75be-e053-2a95a90a34d3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide, Titanium Dioxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Have & Be Co., Ltd.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-10-31
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 2 mg/50mL; mg/50mL
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49404-143 | DR.JART EVERY SUN DAY MINERAL SUN SCREEN (ZINC OXIDE, TITANIUM DIOXIDE) CREAM [HAVE & BE CO., LTD.] | 4 | Legacy NDC | 20240621_33356dd9-44c7-485f-814a-518ab1a29a37.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49404-143-02 | 49404014302 | 1 CONTAINER in 1 CARTON (49404-143-02) > 50 mL in 1 CONTAINER (49404-143-01) | 1 container | 2019-10-31 | 0000-00-00 | No | No | Current |
| 49404-143-03 | 49404014303 | 5 mL in 1 TUBE (49404-143-03) | 5 ml | 2021-12-21 | 0000-00-00 | No | No | Current |