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  5. NDC Package Code: 11822-9600-1 Antifungal Solution Maximum Strength

NDC Package 11822-9600-1 Antifungal Solution Maximum Strength

Tolnaftate Liquid Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
11822-9600-1
Package Description:
1 BOTTLE, WITH APPLICATOR in 1 CARTON / 30 mL in 1 BOTTLE, WITH APPLICATOR
Product Code:
11822-9600
Proprietary Name:
Antifungal Solution Maximum Strength
Non-Proprietary Name:
Tolnaftate
Substance Name:
Tolnaftate
Usage Information:
Tolnaftate is used to treat skin infections such as athlete's foot, jock itch, and ringworm. It is an antifungal that works by preventing the growth of fungus.
11-Digit NDC Billing Format:
11822960001
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Rite Aid Corporation
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
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 10 mg/mL
Sample Package:
No
FDA Application Number:
M005
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
03-12-2024
End Marketing Date:
09-30-2026
Exclude Flag:
N
Code Structure:

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 disclaimer below.

Frequently Asked Questions

What is NDC 11822-9600-1?

The NDC Packaged Code 11822-9600-1 is assigned to a package of 1 bottle, with applicator in 1 carton / 30 ml in 1 bottle, with applicator of Antifungal Solution Maximum Strength, a human over the counter drug labeled by Rite Aid Corporation. The product's dosage form is liquid and is administered via topical form.

Is NDC 11822-9600 included in the NDC Directory?

Yes, Antifungal Solution Maximum Strength with product code 11822-9600 is active and included in the NDC Directory. The product was first marketed by Rite Aid Corporation on March 12, 2024.

What is the 11-digit format for NDC 11822-9600-1?

The 11-digit format is 11822960001. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-4-111822-9600-15-4-211822-9600-01