Anti Itch Soothing 1 Pramoxine Hydrochloride Spray
NDC Package 82637-9370-1

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

Package Information

Anti Itch Soothing 1 Pramoxine Hydrochloride (pramoxine hydrochloride) sprays is adults and children 12 years of age and older: Apply to affected not more than 3 or 4 times daily. This formulation utilizes a spray delivery system. Marketed by The Honey Pot Company Llc, this product is identified by NDC 82637-9370 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
82637-9370-1
Package Description
1 BOTTLE, SPRAY in 1 CARTON / 80 mL in 1 BOTTLE, SPRAY
Product Code
82637-9370
11-Digit Billing Format
82637937001
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Anti Itch Soothing 1 Pramoxine Hydrochloride
Non-Proprietary Name
Pramoxine Hydrochloride
Substance Name
Pramoxine Hydrochloride
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
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)
PRAMOXINE HYDROCHLORIDE 10 mg/mL
Usage Information
Adults and children 12 years of age and older: Apply to affected not more than 3 or 4 times daily. Children under 12 years of age: Consult a doctor

Regulatory & Marketing

Labeler Name
The Honey Pot Company Llc
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-01-2022
Listing Expiration
12-31-2026
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 82637-9370-1 identifies a specific commercial package of 1 bottle, spray in 1 carton / 80 ml in 1 bottle, spray of Anti Itch Soothing 1 Pramoxine Hydrochloride, a human over the counter drug labeled by The Honey Pot Company Llc. This spray is formulated for topical use and contains pramoxine hydrochloride 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 The Honey Pot Company Llc on March 01, 2022. The current certification is valid through December 31, 2026.

How is this The Honey Pot Company Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82637937001. 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 (5-4-1)
82637-9370-1
11-Digit CMS (5-4-2)
82637-9370-01

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