NDC Package 59555-230-18 Ic Ivy Relief

Diphenhydramine Hydrochloride And Zinc Acetate Liquid 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:
59555-230-18
Package Description:
1 mL in 1 PACKET
Product Code:
Proprietary Name:
Ic Ivy Relief
Non-Proprietary Name:
Diphenhydramine Hydrochloride And Zinc Acetate
Substance Name:
Diphenhydramine Hydrochloride; Zinc Acetate
Usage Information:
Do not use more than directedHold stick straight down over infected areapress tip of stick repeatedly on affect skin area until liquid flows, then dab sparinglyadults and children 2 years of age and older: apply to affected area not more then 3 to 4 times dailychildren under 2 years of age: ask a doctor
11-Digit NDC Billing Format:
59555023018
NDC to RxNorm Crosswalk:
  • RxCUI: 1294589 - diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical Solution
  • RxCUI: 1294589 - diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Solution
  • RxCUI: 1294589 - diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    R & R Lotion, 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.
  • Sample Package:
    No
    FDA Application Number:
    part348
    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:
    09-01-2021
    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.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    59555-230-0459 mL in 1 BOTTLE, DISPENSING
    59555-230-07118 mL in 1 BOTTLE, DISPENSING
    59555-230-1920 mL in 1 BOTTLE, WITH APPLICATOR

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 59555-230-18?

    The NDC Packaged Code 59555-230-18 is assigned to a package of 1 ml in 1 packet of Ic Ivy Relief, a human over the counter drug labeled by R & R Lotion, Inc. The product's dosage form is liquid and is administered via topical form.

    Is NDC 59555-230 included in the NDC Directory?

    Yes, Ic Ivy Relief with product code 59555-230 is active and included in the NDC Directory. The product was first marketed by R & R Lotion, Inc on September 01, 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 59555-230-18?

    The 11-digit format is 59555023018. 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
    5-3-259555-230-185-4-259555-0230-18