Foot Odor Control Powder
- Product NDC
- 56104-252
- 11-digit product format
- 561040252
- Labeler code
- 56104
- Product ID
- 56104-252_45c7c11b-d629-aee8-e063-6294a90a401d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- Premier Brands of America Inc.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-09-29
- Substance
- TOLNAFTATE
- Active strength
- 1.3 g/113g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Foot Odor Control Powder
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | 1.3 g/113g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 56104-252-01 | Foot Odor Control Powder | 113 g in 1 CAN | AEROSOL, SPRAY | 113 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 56104-252 | FOOT ODOR CONTROL POWDER (TOLNAFTATE) AEROSOL, SPRAY [PREMIER BRANDS OF AMERICA INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241016_edb0a2da-aaa1-3b9b-e053-2995a90a5012.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 56104-252-01 | 56104025201 | 113 g in 1 CAN (56104-252-01) | 113 g | 2021-09-29 | 0000-00-00 | No | No | Current |