NDC 75525-004 Jd Antiseptic Alcohol 70%

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:
75525-004
Proprietary Name:
Jd Antiseptic Alcohol 70%
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
75525
Start Marketing Date: [9]
10-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 75525-004?

The NDC code 75525-004 is assigned by the FDA to the product Jd Antiseptic Alcohol 70% which is product labeled by Iwanna Corp Sas. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 75525-004-01 3800 ml in 1 bottle, plastic , 75525-004-05 18900 ml in 1 bottle, plastic , 75525-004-10 1000 ml in 1 bottle, plastic , 75525-004-50 500 ml in 1 bottle, plastic , 75525-004-55 208000 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 Jd Antiseptic Alcohol 70%?

Clean affected areaApply a small amount of this product on the area 1-3 times dailyIf bandaged, let dry firstMay be covered with a sterile bandage

Which are Jd Antiseptic Alcohol 70% UNII Codes?

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

Which are Jd Antiseptic Alcohol 70% 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".