Scrubs Sunscren
- Product NDC
- 51239-3921
- 11-digit product format
- 512393921
- Labeler code
- 51239
- Product ID
- 51239-3921_dd0a0777-8a7b-0ed3-e053-2995a90af5b1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sunscreen
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- ITW Pro Brands
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-12-01
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 0 g/g; g/g; g/g; g/g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 51239-3921-0 | 51239392100 | 7 g in 1 POUCH (51239-3921-0) | 7 g | 2021-12-01 | 0000-00-00 | No | No | Current |
| 51239-3921-1 | 51239392101 | 100 PACKET in 1 CARTON (51239-3921-1) > 7 g in 1 PACKET | 100 packet | 2021-12-01 | 0000-00-00 | No | No | Current |