Ludens
- Product NDC
- 52183-227
- 11-digit product format
- 521830227
- Labeler code
- 52183
- Product ID
- 52183-227_6bdb13ca-0e1c-4c4c-b800-8eabe6980e1c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- pectin and menthol
- Dosage form
- LOZENGE
- Route
- ORAL
- Labeler
- Prestige Brands Holdings, Inc.
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-06-15
- Substance
- MENTHOL; PECTIN
- Active strength
- 2.5; 2.8 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ludens
- Brand name suffix
- Dual Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 2.5 mg/1 |
| PECTIN | 2.8 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A, 89NA02M4RX |
| Rxcui | 2056063, 2056069 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52183-227-25 | LudensDual Relief | 25 in 1 BAG | LOZENGE | 25 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52183-227 | LUDENS DUAL RELIEF (PECTIN AND MENTHOL) LOZENGE [PRESTIGE BRANDS HOLDINGS, INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20241113_d0213cb3-ec8e-40cc-82c9-694032f0490f.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 |
|---|
| 52183-227-25 | 52183022725 | 25 LOZENGE in 1 BAG (52183-227-25) | 25 lozenge | 2018-06-15 | 0000-00-00 | No | No | Current |