Bitemd External Analgesic First Aid Antiseptic Liquid
NDC Package 79364-0932-1

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

Package Information

Bitemd External Analgesic First Aid Antiseptic (benzocaine, camphor (synthetic), and phenol) liquids is clean area.Apply to the bite area by pressing straight down repeatedly until liquid flows, then dab sparingly.If itching persists, apply again in 10 to 15 minutes.For ticks and bees, remove tick or stinger before treatment. This formulation utilizes a liquid delivery system. Marketed by United Industries Corporation, this product is identified by NDC 79364-0932 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
79364-0932-1
Package Description
14.7 mL in 1 BOTTLE
Product Code
79364-0932
11-Digit Billing Format
79364093201

Clinical Specifications

Proprietary Name
Bitemd External Analgesic First Aid Antiseptic
Non-Proprietary Name
Benzocaine, Camphor (synthetic), And Phenol
Substance Name
Benzocaine; Camphor (synthetic); Phenol
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
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
Clean area.Apply to the bite area by pressing straight down repeatedly until liquid flows, then dab sparingly.If itching persists, apply again in 10 to 15 minutes.For ticks and bees, remove tick or stinger before treatment.

Regulatory & Marketing

Labeler Name
United Industries Corporation
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-01-2020
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 79364-0932-1 identifies a specific commercial package of 14.7 ml in 1 bottle of Bitemd External Analgesic First Aid Antiseptic, a human over the counter drug labeled by United Industries Corporation. This liquid is formulated for topical use and contains benzocaine; camphor (synthetic); phenol 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 United Industries Corporation on January 01, 2020. The current certification is valid through December 31, 2026.

How is this United Industries Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 79364093201. 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)
79364-0932-1
11-Digit CMS (5-4-2)
79364-0932-01

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