Fluopar
- Product NDC
- 59088-754
- 11-digit product format
- 590880754
- Labeler code
- 59088
- Product ID
- 59088-754_292ff5ee-68a5-7a8c-e063-6294a90a29e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fluocinonide, dimethicone
- Dosage form
- KIT
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2014-01-14
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 59088-754-00 | 59088075400 | 1 KIT in 1 KIT (59088-754-00) * 1 TUBE in 1 CARTON (45802-151-94) / 30 g in 1 TUBE * 118 mL in 1 TUBE (59088-333-08) | 1 kit | 2020-03-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Fluopar | PureTek Corporation | Perrigo New York Inc | 2024-12-13 | HUMAN PRESCRIPTION DRUG LABEL | 5 |