Urea
- Product NDC
- 52191-351
- 11-digit product format
- 521910351
- Labeler code
- 52191
- Product ID
- 52191-351_69ac5657-d5b3-1abc-e053-2991aa0a26d7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- UREA
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Bowyn Labs, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2018-04-12
- Marketing end
- 0000-00-00
- Substance
- UREA
- Active strength
- 410 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 52191-351-08 | 52191035108 | 227 g in 1 BOTTLE, PLASTIC (52191-351-08) | 227 g | 2018-04-12 | 0000-00-00 | No | No | Current |