Curasore
- Product NDC
- 12258-223
- 11-digit product format
- 122580223
- Labeler code
- 12258
- Product ID
- 12258-223_47e0a9b6-4f7a-b034-e063-6394a90a64ba
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pramoxine Hydrochloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- S.S.S. Company
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1995-08-31
- Substance
- PRAMOXINE HYDROCHLORIDE
- Active strength
- 1 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Curasore
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PRAMOXINE HYDROCHLORIDE | 1 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 88AYB867L5 |
| Rxcui | 1294034, 2109512 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 12258-223-05 | Curasore | 15 mL in 1 BOTTLE | LIQUID | 15 | | 7 |
| 12258-223-05 | Curasore | 1 in 1 CARTON | LIQUID | 1 | | 7 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 12258-223 | CURASORE (PRAMOXINE HYDROCHLORIDE) LIQUID [S.S.S. COMPANY] | 6 | Current NDC, Legacy NDC, 2 package rows | 20250119_6891e5aa-e6f2-4355-8ee9-d23c9959787e.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 |
|---|
| 12258-223-05 | 12258022305 | 1 BOTTLE in 1 CARTON (12258-223-05) / 15 mL in 1 BOTTLE | 1 bottle | 1995-08-31 | 0000-00-00 | No | No | Current |