Medi-first Tolnaftate 1% Antifungal Cream
NDC Package 47682-862-70
Package Information
Medi-first Tolnaftate 1% Antifungal Cream is directionswash affected area and dry thoroughlyapply a thin layer over affected area twice daily (morning and night) or as directed by a doctorsupervise children in the use of this productfor athlete's foot, pay special attention to spaces between the toes, wear well-fitting, ventilated shoes, and change shoes and socks at least once dailyfor athlete's foot and ringworm use daily for 4 weeks, for jock itch use daily for 2 weeks; if condition persists longer, ask a doctor. Marketed by Unifirst First Aid Corporation, this product is identified by NDC 47682-862 and is authorized under FDA application M005.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 47682 - Unifirst First Aid Corporation
- 47682-862 - Medi-first Tolnaftate 1% Antifungal Cream
- 47682-862-70 - 4 TUBE in 1 BOX / 35.4 g in 1 TUBE
- 47682-862 - Medi-first Tolnaftate 1% Antifungal Cream
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (47682-862). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 47682-862-70 identifies a specific commercial package of 4 tube in 1 box / 35.4 g in 1 tube of Medi-first Tolnaftate 1% Antifungal Cream, labeled by Unifirst First Aid Corporation. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Unifirst First Aid Corporation on November 01, 2025. The current certification is valid through June 16, 2026.
How is this Unifirst First Aid Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 47682086270. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.
