Tolnaftate
- Product NDC
- 56104-008
- 11-digit product format
- 561040008
- Labeler code
- 56104
- Product ID
- 56104-008_c7045d71-6ba2-59f1-e053-2995a90a7c8d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Foot Odor Control Spray Powder
- Dosage form
- AEROSOL, POWDER
- Route
- TOPICAL
- Labeler
- Premier Brands of America Inc.
- Application
- part333C
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2013-01-01
- Marketing end
- 0000-00-00
- Substance
- TOLNAFTATE
- Active strength
- 1 g/113g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 56104-008-04 | 56104000804 | 113 g in 1 CANISTER (56104-008-04) | 113 g | 2013-01-01 | 0000-00-00 | No | No | Current |