GoodSense Menthol Cough Drops
- Product NDC
- 50804-013
- 11-digit product format
- 508040013
- Labeler code
- 50804
- Product ID
- 50804-013_45c83b66-9631-6b48-e063-6294a90a44b2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- LOZENGE
- Route
- ORAL
- Labeler
- Geiss, Destin, Dunn
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-07-09
- Substance
- MENTHOL
- Active strength
- 5.4 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
- GoodSense Menthol Cough Drops
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 5.4 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 485287 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50804-013-30 | GoodSense Menthol Cough Drops | 30 in 1 BAG | LOZENGE | 30 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50804-013 | GOODSENSE MENTHOL COUGH DROPS (MENTHOL) LOZENGE [GEISS, DESTIN, DUNN] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241202_c6b25d69-8930-6867-e053-2a95a90ad208.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 |
|---|
| 50804-013-30 | 50804001330 | 30 LOZENGE in 1 BAG (50804-013-30) | 30 lozenge | 2021-07-09 | 0000-00-00 | No | No | Current |