Licefreee AfterLice
- Product NDC
- 51879-260
- 11-digit product format
- 518790260
- Labeler code
- 51879
- Product ID
- 51879-260_262f50ab-fd53-7474-e063-6394a90a4f40
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pramoxine HCI
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Tec Laboratories Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-10-16
- Substance
- PRAMOXINE HYDROCHLORIDE
- Active strength
- 10 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Licefreee AfterLice
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PRAMOXINE HYDROCHLORIDE | 10 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 88AYB867L5 |
| Rxcui | 1294036 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51879-260-06 | Licefreee AfterLice | 177.4 g in 1 BOTTLE, PLASTIC | SPRAY | 177.4 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51879-260 | LICEFREEE AFTERLICE (PRAMOXINE HCI) SPRAY [TEC LABORATORIES INC.] | 2 | Current NDC, 1 package rows | 20241107_06c4cc42-a215-3949-e063-6394a90a665e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51879-260-06 | 51879026006 | 177.4 g in 1 BOTTLE, PLASTIC (51879-260-06) | 177.4 g | 2023-10-16 | No | No | Current |