K19 RELIEF
- Product NDC
- 83574-413
- 11-digit product format
- 835740413
- Labeler code
- 83574
- Product ID
- 83574-413_2bbc8ed1-176c-27a5-e063-6394a90a38ee
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- K19 LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-07-10
- Substance
- MENTHOL
- Active strength
- 12.5 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83574-413-00 | 83574041300 | 295 mL in 1 BOTTLE, SPRAY (83574-413-00) | 295 ml | 2023-07-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| K19 SPRAY RELIEF | K19 LLC | 2025-01-15 | HUMAN OTC DRUG LABEL | 3 |