NDC 12745-109 Compound Benzoin Tincture

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
12745-109
Proprietary Name:
Compound Benzoin Tincture
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Medical Chemical Corporation
Labeler Code:
12745
Start Marketing Date: [9]
06-15-1954
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 12745-109-01

Package Description: 59 mL in 1 BOTTLE

NDC Code 12745-109-02

Package Description: 118 mL in 1 BOTTLE, GLASS

NDC Code 12745-109-03

Package Description: 118 mL in 1 BOTTLE, SPRAY

NDC Code 12745-109-04

Package Description: 473 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 12745-109?

The NDC code 12745-109 is assigned by the FDA to the product Compound Benzoin Tincture which is product labeled by Medical Chemical Corporation. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 12745-109-01 59 ml in 1 bottle , 12745-109-02 118 ml in 1 bottle, glass , 12745-109-03 118 ml in 1 bottle, spray , 12745-109-04 473 ml in 1 bottle, plastic . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Compound Benzoin Tincture?

Directions: Apply to affected area for first-aid treatment of minor cuts and abrasions.  Discontinue use and get medical aid if redness, irritation or infection develops.  In case of deep or puncture wounds consult a physician.

Which are Compound Benzoin Tincture UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Compound Benzoin Tincture Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Compound Benzoin Tincture?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".