Sunscreen
- Product NDC
- 51414-906
- Requested package NDC
- 51414-906-01
- 11-digit product format
- 514140906
- Labeler code
- 51414
- Product ID
- 51414-906_da8b491b-bc8b-a5b1-e053-2a95a90acfad
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate,oxybenzone,OCTISALATE,Titanium dioxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Yuyao Jessie Commodity Co.,Ltd.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2012-09-12
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE
- Active strength
- 7 g/100g; g/100g; g/100g; g/100g
- 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 |
|---|---|---|---|---|---|---|---|---|
| 51414-906-01 | 51414090601 | 5 g in 1 BOTTLE (51414-906-01) | 5 g | 2016-12-11 | 0000-00-00 | No | No | Current |