Sunscreen
- Product NDC
- 51414-907
- Requested package NDC
- 51414-907-08
- 11-digit product format
- 514140907
- Labeler code
- 51414
- Product ID
- 51414-907_da8b1d01-44f0-f1ef-e053-2995a90aa943
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octocrylene ,Homosalate,Avobenzone,Octisalate
- 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
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 3 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 |
|---|---|---|---|---|---|---|---|---|
| 51414-907-08 | 51414090708 | 50 g in 1 BOTTLE (51414-907-08) | 50 g | 2016-12-11 | 0000-00-00 | No | No | Current |