Tolnaftate Aerosol, Spray
NDC Package 42507-415-01
Package Information
Tolnaftate (antifungal liquid spray) aerosols is wash affected area and dry thoroughlyshake can well and spray a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctorto prevent athlete's foot, shake can well and spray a thin layer of the product to the feet once or twice daily (morning and/or night)supervise 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 weeksif condition persists, consult a doctorthis product is not effective on the scalp or nails. This formulation utilizes a aerosol, spray delivery system. Marketed by Hy-vee, Inc, this product is identified by NDC 42507-415 and is authorized under FDA application M005.
Identification & Billing
- RxCUI: 313421 - tolnaftate 1 % Topical Spray
- RxCUI: 313421 - tolnaftate 10 MG/ML Topical Spray
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 42507 - Hy-vee, Inc
- 42507-415 - Tolnaftate
- 42507-415-01 - 150 g in 1 CANISTER
- 42507-415 - Tolnaftate
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 42507-415-01 identifies a specific commercial package of 150 g in 1 canister of Tolnaftate, a human over the counter drug labeled by Hy-vee, Inc. This aerosol, spray is formulated for topical use and contains tolnaftate as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Hy-vee, Inc on October 16, 2025. The current certification is valid through December 31, 2026.
How is this Hy-vee, Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 42507041501. 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.