Benzoin Tincture Liquid
NDC Package 70677-1200-1

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

Package Information

Benzoin Tincture (benzoin resin) liquids is adult and children 6 months of age and older: Dry the affected area. This formulation utilizes a liquid delivery system. Marketed by 116956644, this product is identified by NDC 70677-1200 and is authorized under FDA application M022.

Identification & Billing

NDC Package Code
70677-1200-1
Package Description
59 mL in 1 BOTTLE, GLASS
Product Code
70677-1200
11-Digit Billing Format
70677120001

Clinical Specifications

Proprietary Name
Benzoin Tincture
Non-Proprietary Name
Benzoin Resin
Substance Name
Benzoin Resin
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)
BENZOIN RESIN 1000 mg/mL
Usage Information
Adult and children 6 months of age and older: Dry the affected area. Saturate a cotton applicator with medication and apply undiluted to the affected area not more than every 2 hours.Children under 6 months of age: Consult a dentist or doctor.

Regulatory & Marketing

Labeler Name
116956644
Product Type
Human Otc Drug
FDA Application #
M022
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
12-17-2024
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 70677-1200-1 identifies a specific commercial package of 59 ml in 1 bottle, glass of Benzoin Tincture, a human over the counter drug labeled by 116956644. This liquid is formulated for topical use and contains benzoin resin 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 116956644 on December 17, 2024. The current certification is valid through December 31, 2026.

How is this 116956644 product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70677120001. 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)
70677-1200-1
11-Digit CMS (5-4-2)
70677-1200-01

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