1. Home
  2. Labeler Index
  3. Acuity Specialty Products, Inc Dba Afco Us
  4. 68776-1001
  5. NDC Package Code: 68776-1001-2 Wyandotte Sanifect E3

NDC Package 68776-1001-2 Wyandotte Sanifect E3

Alcohol Lotion 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:
68776-1001-2
Package Description:
208 L in 1 DRUM
Product Code:
68776-1001
Proprietary Name:
Wyandotte Sanifect E3
Non-Proprietary Name:
Alcohol
Substance Name:
Alcohol
Usage Information:
Place a palmful of product in one hand. Spread on both hands and rub into the skin until dry (1 - 2 min.). No rinsing or toweling required
11-Digit NDC Billing Format:
68776100102
NDC to RxNorm Crosswalk:
  • RxCUI: 1537437 - ethanol 60.1 % Topical Lotion
  • RxCUI: 1537437 - ethanol 0.601 ML/ML Topical Lotion
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Acuity Specialty Products, Inc Dba Afco Us
    Dosage Form:
    Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
    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):
  • ALCOHOL 60.1 L/100L
    • Sample Package:
    No
    FDA Application Number:
    M007
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    10-01-2006
    Listing Expiration Date:
    12-31-2024
    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
    68776-1001-13.784 L in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 68776-1001-2?

    The NDC Packaged Code 68776-1001-2 is assigned to a package of 208 l in 1 drum of Wyandotte Sanifect E3, a human over the counter drug labeled by Acuity Specialty Products, Inc Dba Afco Us. The product's dosage form is lotion and is administered via topical form.

    Is NDC 68776-1001 included in the NDC Directory?

    Yes, Wyandotte Sanifect E3 with product code 68776-1001 is active and included in the NDC Directory. The product was first marketed by Acuity Specialty Products, Inc Dba Afco Us on October 01, 2006 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68776-1001-2?

    The 11-digit format is 68776100102. 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
    5-4-168776-1001-25-4-268776-1001-02