Clear Anti-itch Lotion
NDC Package 83324-245-06

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Clear Anti-itch (pramoxine hcl, zinc acetate) lotions is shake well  before applying wash affected area of skinadults and children 2 years of age and older - apply to affected area no more than 3 to 4 times dailychildren under 2 years - ask a doctor. This formulation utilizes a lotion delivery system. Marketed by Chain Drug Marketing Association, this product is identified by NDC 83324-245 and is authorized under FDA application M016.

Identification & Billing

NDC Package Code
83324-245-06
Package Description
177 mL in 1 BOTTLE, PLASTIC
Product Code
83324-245
11-Digit Billing Format
83324024506
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Units Per Package
177 ML
RxNorm Crosswalk
  • RxCUI: 1234546 - pramoxine HCl 1 % / zinc acetate 0.1 % Topical Lotion
  • RxCUI: 1234546 - pramoxine hydrochloride 10 MG/ML / zinc acetate 1 MG/ML Topical Lotion

Clinical Specifications

Proprietary Name
Clear Anti-itch
Non-Proprietary Name
Pramoxine Hcl, Zinc Acetate
Substance Name
Pramoxine Hydrochloride; Zinc Acetate
Dosage Form
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
Administration Route
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)
Pharmacologic Class
Usage Information
Shake well  before applying wash affected area of skinadults and children 2 years of age and older - apply to affected area no more than 3 to 4 times dailychildren under 2 years - ask a doctor

Regulatory & Marketing

Labeler Name
Chain Drug Marketing Association
Product Type
Human Otc Drug
FDA Application #
M016
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-26-2025
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 83324-245-06 identifies a specific commercial package of 177 ml in 1 bottle, plastic of Clear Anti-itch, a human over the counter drug labeled by Chain Drug Marketing Association. This lotion is formulated for topical use and contains pramoxine hydrochloride; zinc acetate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Chain Drug Marketing Association on February 26, 2025. The current certification is valid through December 31, 2027.

How is this Chain Drug Marketing Association product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83324024506. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. There are 177 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
83324-245-06
11-Digit CMS (5-4-2)
83324-0245-06

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.