Anesgerm La Muela Liquid
NDC Package 73635-7101-5

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

Package Information

Anesgerm La Muela (benzocaine 20%) liquids is adults & children, 12 yrs of age & older ■ Apply to the affected area up to 4 times daily or as directed by a dentist or doctor. This formulation utilizes a liquid delivery system. Marketed by Germa Products, Llc, this product is identified by NDC 73635-7101 and is authorized under FDA application M022.

Identification & Billing

NDC Package Code
73635-7101-5
Package Description
1 BOTTLE, WITH APPLICATOR in 1 BOX / 14.8 mL in 1 BOTTLE, WITH APPLICATOR
Product Code
73635-7101
11-Digit Billing Format
73635710105
RxNorm Crosswalk
  • RxCUI: 308657 - benzocaine 20 % Mucous Membrane Topical Solution
  • RxCUI: 308657 - benzocaine 200 MG/ML Mucous Membrane Topical Solution

Clinical Specifications

Proprietary Name
Anesgerm La Muela Fast Pain Relief
Non-Proprietary Name
Benzocaine 20%
Substance Name
Benzocaine
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)
BENZOCAINE 200 mg/mL
Pharmacologic Class
Usage Information
Adults & children, 12 yrs of age & older ■ Apply to the affected area up to 4 times daily or as directed by a dentist or doctor. Children 2 yrs of age & older ■ As directed by a dentist or doctor. Children under 2 years of age ■ Do not use.

Regulatory & Marketing

Labeler Name
Germa Products, Llc
Product Type
Human Otc Drug
FDA Application #
M022
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-29-2019
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 73635-7101-5 identifies a specific commercial package of 1 bottle, with applicator in 1 box / 14.8 ml in 1 bottle, with applicator of Anesgerm La Muela Fast Pain Relief, a human over the counter drug labeled by Germa Products, Llc. This liquid is formulated for topical use and contains benzocaine 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 Germa Products, Llc on March 29, 2019. The current certification is valid through December 31, 2026.

How is this Germa Products, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73635710105. 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)
73635-7101-5
11-Digit CMS (5-4-2)
73635-7101-05

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