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  4. NDC Product Code: 0395-9107 Benzoin Tincture

NDC 0395-9107 Benzoin Tincture

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 0395-9107?
  4. Benzoin Tincture Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
0395-9107
Proprietary Name:
Benzoin Tincture
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Humco Holding Group, Inc.
Labeler Code:
0395
Product Label ID:
60517f09-674c-ea0c-e053-2991aa0a9b92
Start Marketing Date: [9]
01-01-2008
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 0395-9107?

The NDC code 0395-9107 is assigned by the FDA to the product Benzoin Tincture which is product labeled by Humco Holding Group, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0395-9107-92 59 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 Benzoin Tincture?

Adults and children 6 months of age and older: Dry the affected area, with cotton swab, apply undiluted to the affected area not more often than every 2 hours.Children under 6 months of age: Consult a dentiest or doctor.

Which are Benzoin Tincture UNII Codes?

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

Which are 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:

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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".