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  5. NDC Package Code: 61010-8600-1 Saniwash Antimicrobial Foaming Hand

NDC Package 61010-8600-1 Saniwash Antimicrobial Foaming Hand

Chloroxylenol 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:
61010-8600-1
Package Description:
550 mL in 1 BOTTLE, PUMP
Product Code:
61010-8600
Proprietary Name:
Saniwash Antimicrobial Foaming Hand
Non-Proprietary Name:
Chloroxylenol
Substance Name:
Chloroxylenol
Usage Information:
Wet hands and forearms. Apply 5 millimeters (teaspoonful) or palmful to hand and forearm. Scrub thoroughly for 30 seconds. Rince and repeat.
11-Digit NDC Billing Format:
61010860001
NDC to RxNorm Crosswalk:
  • RxCUI: 413262 - chloroxylenol 0.6 % Medicated Liquid Soap
  • RxCUI: 413262 - chloroxylenol 6 MG/ML Medicated Liquid Soap
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Safetec Of America, Inc.
    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 .006 g/mL
    • Sample Package:
    No
    FDA Application Number:
    505G(a)(3)
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    03-13-2014
    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.

    Frequently Asked Questions

    What is NDC 61010-8600-1?

    The NDC Packaged Code 61010-8600-1 is assigned to a package of 550 ml in 1 bottle, pump of Saniwash Antimicrobial Foaming Hand, a human over the counter drug labeled by Safetec Of America, Inc.. The product's dosage form is liquid and is administered via topical form.

    Is NDC 61010-8600 included in the NDC Directory?

    Yes, Saniwash Antimicrobial Foaming Hand with product code 61010-8600 is active and included in the NDC Directory. The product was first marketed by Safetec Of America, Inc. on March 13, 2014 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 61010-8600-1?

    The 11-digit format is 61010860001. 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
    5-4-161010-8600-15-4-261010-8600-01