Scrubs Sunscreen
- Product NDC
- 51239-1921
- 11-digit product format
- 512391921
- Labeler code
- 51239
- Product ID
- 51239-1921_d24263cc-d418-61fb-e053-2995a90a4e22
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sunscreen
- Dosage form
- LOTION
- Route
- CUTANEOUS
- Labeler
- ITW Pro Brands
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-05-01
- Marketing end
- 2023-09-08
- Substance
- OCTISALATE; OXYBENZONE; HOMOSALATE; OCTINOXATE; AVOBENZONE
- Active strength
- 0 g/g; g/g; g/g; g/g; g/g
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51239-1921-0 | 51239192100 | 7 g in 1 POUCH (51239-1921-0) | 7 g | 2017-05-01 | 0000-00-00 | No | No | Current |