Tolnaftate Aerosol, Spray
NDC Package 11822-0780-5

11-digit billing NDC: 11822078005
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

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 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 if condition persists, consult a doctorto prevent athlete's foot: wash the feet and dry thoroughly; spray a thin layer of the product to the feet once or twice daily (morning and/or night)this product is not effective on the scalp or nailsif nozzle clogs, clean with a pin. This formulation utilizes a aerosol, spray delivery system. Marketed by Rite Aid Corporation, this product is identified by NDC 11822-0780 and is authorized under FDA application M005.

Identification & Billing

NDC Package Code
11822-0780-5
Package Description
150 g in 1 CANISTER
Product Code
11822-0780
11-Digit Billing Format
11822078005
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Tolnaftate
Non-Proprietary Name
Antifungal Liquid Spray
Substance Name
Tolnaftate
Dosage Form
Aerosol, Spray - An aerosol product which utilizes a compressed gas as the propellant to provide the force necessary to expel the product as a wet spray; it is applicable to solutions of medicinal agents in aqueous solvents.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
TOLNAFTATE 1.5 g/150g
Usage Information
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 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 if condition persists, consult a doctorto prevent athlete's foot: wash the feet and dry thoroughly; spray a thin layer of the product to the feet once or twice daily (morning and/or night)this product is not effective on the scalp or nailsif nozzle clogs, clean with a pin

Regulatory & Marketing

Labeler Name
Rite Aid Corporation
Product Type
Human Otc Drug
FDA Application #
M005
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-01-2021
End Marketing Date
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 11822-0780-5 identifies a specific commercial package of 150 g in 1 canister of Tolnaftate, a human over the counter drug labeled by Rite Aid Corporation. 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 Rite Aid Corporation on February 01, 2021.

How is this Rite Aid Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 11822078005. 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:

10-Digit Format (5-4-1)
11822-0780-5
11-Digit CMS (5-4-2)
11822-0780-05

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.