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  5. NDC Package Code: 49681-400-04 Lusti Skin Softening Hand Sanitizer

NDC Package 49681-400-04 Lusti Skin Softening Hand Sanitizer

Ethyl Alcohol 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:
49681-400-04
Package Description:
118 mL in 1 BOTTLE
Product Code:
49681-400
Proprietary Name:
Lusti Skin Softening Hand Sanitizer
Non-Proprietary Name:
Ethyl Alcohol
Substance Name:
Alcohol
Usage Information:
This product is used as Antiseptic
11-Digit NDC Billing Format:
49681040004
NDC to RxNorm Crosswalk:
  • RxCUI: 884783 - ethanol 65 % Topical Solution
  • RxCUI: 884783 - ethanol 0.65 ML/ML Topical Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    New Life Products, 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):
  • ALCOHOL 65 mL/100mL
    • Sample Package:
    No
    FDA Application Number:
    part333A
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    05-25-2020
    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.

    Frequently Asked Questions

    What is NDC 49681-400-04?

    The NDC Packaged Code 49681-400-04 is assigned to a package of 118 ml in 1 bottle of Lusti Skin Softening Hand Sanitizer, a human over the counter drug labeled by New Life Products, Inc.. The product's dosage form is liquid and is administered via topical form.

    Is NDC 49681-400 included in the NDC Directory?

    Yes, Lusti Skin Softening Hand Sanitizer with product code 49681-400 is active and included in the NDC Directory. The product was first marketed by New Life Products, Inc. on May 25, 2020 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 49681-400-04?

    The 11-digit format is 49681040004. 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 5-3-2 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
    5-3-249681-400-045-4-249681-0400-04