NDC Package 81923-197-00 Intimale Maximum Strength Delay

Lidocaine Hydrochloride Solution Topical - View Billable Units, 11-Digit Format, RxNorm

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:
81923-197-00
Package Description:
1 CYLINDER in 1 BOX / 15 mL in 1 CYLINDER
Product Code:
Proprietary Name:
Intimale Maximum Strength Delay
Non-Proprietary Name:
Lidocaine Hydrochloride
Substance Name:
Lidocaine Hydrochloride
Usage Information:
Apply 3-5 minutes prior to intercourse. Shake gently before use. Apply 3 or more sprays to the head and shaft of the penis depending on the level of anaesthesia desired.  DO NOT exceed 10 sprays. Massage into the penis for around twenty seconds or until product is completely absorption is reached. Wash hands thoroughly after use. You will feel the product start to work after 3-5 minutes. If you do not experience the desired effect after the product has completely absorbed into the skin, gradually increase the dosage until the desired effect has been achieved. You should always use minimum effective quantity.
11-Digit NDC Billing Format:
81923019700
Product Type:
Human Otc Drug
Labeler Name:
Skins Sexual Health Limited
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
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):
    Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    05-25-2021
    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.

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    Frequently Asked Questions

    What is NDC 81923-197-00?

    The NDC Packaged Code 81923-197-00 is assigned to a package of 1 cylinder in 1 box / 15 ml in 1 cylinder of Intimale Maximum Strength Delay, a human over the counter drug labeled by Skins Sexual Health Limited. The product's dosage form is solution and is administered via topical form.

    Is NDC 81923-197 included in the NDC Directory?

    Yes, Intimale Maximum Strength Delay with product code 81923-197 is active and included in the NDC Directory. The product was first marketed by Skins Sexual Health Limited on May 25, 2021 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 81923-197-00?

    The 11-digit format is 81923019700. 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
    5-3-281923-197-005-4-281923-0197-00