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  5. NDC Package Code: 68776-1005-2 Wyandotte Sanifect Foam-e Ii

NDC Package 68776-1005-2 Wyandotte Sanifect Foam-e Ii

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
68776-1005-2
Package Description:
18927.1 mL in 1 JUG
Product Code:
68776-1005
Proprietary Name:
Wyandotte Sanifect Foam-e Ii
Non-Proprietary Name:
Chloroxylenol
Substance Name:
Chloroxylenol
Usage Information:
Directions:For one step hand washing and sanitizing, wet hands with water. Apply a generous amount of product in palm of hand and work into lather. Rinse thoroughly with potable water. Dry hands completely.
11-Digit NDC Billing Format:
68776100502
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Acuity Specialty Products, Inc Dba Afco Us
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):
CHLOROXYLENOL 2081980 mg/208198mL
Sample Package:
No
FDA Application Number:
M003
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
01-06-2009
Listing Expiration Date:
12-31-2025
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
68776-1005-13785.41 mL in 1 JUG
68776-1005-3208198 mL in 1 DRUM

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 68776-1005-2?

The NDC Packaged Code 68776-1005-2 is assigned to a package of 18927.1 ml in 1 jug of Wyandotte Sanifect Foam-e Ii, a human over the counter drug labeled by Acuity Specialty Products, Inc Dba Afco Us. The product's dosage form is liquid and is administered via topical form.

Is NDC 68776-1005 included in the NDC Directory?

Yes, Wyandotte Sanifect Foam-e Ii with product code 68776-1005 is active and included in the NDC Directory. The product was first marketed by Acuity Specialty Products, Inc Dba Afco Us on January 06, 2009 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 68776-1005-2?

The 11-digit format is 68776100502. 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
5-4-168776-1005-25-4-268776-1005-02