SUNSCREEN
- Product NDC
- 51414-905
- Requested package NDC
- 51414-905-10
- 11-digit product format
- 514140905
- Labeler code
- 51414
- Product ID
- 51414-905_da8b7c91-74fb-3c9b-e053-2995a90ac715
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate,ZINC OXIDE,OCTISALATE
- Dosage form
- STICK
- Route
- TOPICAL
- Labeler
- Yuyao Jessie Commodity Co.,Ltd.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-05-08
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE; ZINC OXIDE
- Active strength
- 3 g/100g; g/100g; g/100g
- 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
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 51414-905-10 | 51414090510 | 2 g in 1 PACKAGE (51414-905-10) | 2 g | 2018-01-05 | 0000-00-00 | No | No | Current |