Menthol
- Product NDC
- 81522-069
- 11-digit product format
- 815220069
- Labeler code
- 81522
- Product ID
- 81522-069_422aaf23-440e-34a8-e063-6294a90a215d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Maximum Strength Medicated Foot Powder Talc Free
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- FSA Store Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-05-02
- Substance
- MENTHOL
- 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
- Menthol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 10 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 259579 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81522-069-01 | Menthol | 283 g in 1 BOTTLE, PLASTIC | POWDER | 283 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81522-069 | MENTHOL (MAXIMUM STRENGTH MEDICATED FOOT POWDER TALC FREE) POWDER [FSA STORE INC.] | 3 | Current NDC, 1 package rows | 20241109_fb3548c8-f202-dc50-e053-6394a90a5b30.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 |
|---|
| 81522-069-01 | 81522006901 | 283 g in 1 BOTTLE, PLASTIC (81522-069-01) | 283 g | 2023-05-02 | No | No | Historical |