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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Fluopar
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 259090, 485647 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 45802-151-94 | Fluopar | 1 in 1 CARTON | CREAM | | 1 mg in 1g | 5 |
| 45802-151-94 | Fluopar | 30 g in 1 TUBE | CREAM | 30 g | 1 mg in 1g | 5 |
| 59088-333-08 | Fluopar | 118 mL in 1 TUBE | CREAM | 118 mL | 50 mg in 1mL | 5 |
| 59088-754-00 | Fluopar | 1 in 1 KIT | KIT | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59088-754 | FLUOPAR (FLUOCINONIDE, DIMETHICONE) KIT [PURETEK CORPORATION] | 5 | Current NDC, Legacy NDC, 4 package rows | 20241215_9ff7fa78-0fca-976f-e053-2995a90a4641.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 45802-151-94 | 45802015194 | 1 in 1 CARTON | | | | | | Historical |
| 59088-333-08 | 59088033308 | 118 mL in 1 TUBE | 118 ml | | | | | Historical |
| 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 | 0000-00-00 | No | No | Current |