SUNSCREEN
- Product NDC
- 66538-101
- Requested package NDC
- 66538-101-12
- 11-digit product format
- 665380101
- Labeler code
- 66538
- Product ID
- 66538-101_492a7e98-f604-48b4-8540-b8f7e4e7b1a3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE ZINC OXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- COSMOCEUTICAL RESEARCH CENTER INC
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2011-11-28
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; ZINC OXIDE
- Active strength
- 8 g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 66538-101-12 | 66538010112 | 50 g in 1 JAR (66538-101-12) | 50 g | 2011-11-28 | 0000-00-00 | No | No | Current |