Menthol
- Product NDC
- 82442-211
- 11-digit product format
- 824420211
- Labeler code
- 82442
- Product ID
- 82442-211_42f3fbdb-8110-35e8-e063-6394a90a5f53
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Maximum Strength Medicated Foot Powder Talc Free
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Target Corporation
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-05-27
- Substance
- MENTHOL
- Active strength
- 10 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82442-211-01 | Menthol | 283 g in 1 BOTTLE, PLASTIC | POWDER | 283 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82442-211-01 | 82442021101 | 283 g in 1 BOTTLE, PLASTIC (82442-211-01) | 283 g | 2025-05-27 | No | No | Historical |