Maximum Strength Medicated Foot Powder
- Product NDC
- 42669-283
- 11-digit product format
- 426690283
- Labeler code
- 42669
- Product ID
- 42669-283_9df9d907-df74-40b5-8462-c90a3e2e288d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Davion, Inc
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-01-30
- Substance
- MENTHOL
- Active strength
- 1 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Maximum Strength Medicated Foot Powder
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 1 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 259579 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42669-283-01 | Maximum Strength Medicated Foot Powder | 283 g in 1 BOTTLE | POWDER | 283 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42669-283 | MAXIMUM STRENGTH MEDICATED FOOT POWDER (MENTHOL) POWDER [DAVION, INC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240229_7b442d99-ac19-4f65-828d-954c5350ef5a.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 |
|---|
| 42669-283-01 | 42669028301 | 283 g in 1 BOTTLE (42669-283-01) | 283 g | 2018-01-30 | 0000-00-00 | No | No | Current |