NDC 76725-012 Dr Clinic 75% Alcohol Wipes

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:
76725-012
Proprietary Name:
Dr Clinic 75% Alcohol Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
76725
Start Marketing Date: [9]
09-10-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 76725-012?

The NDC code 76725-012 is assigned by the FDA to the product Dr Clinic 75% Alcohol Wipes which is product labeled by Makyaj Kozmetik Insaat Sanayi Ve Ticaret Limited Sirketi. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 76725-012-01 80 package in 1 canister / 2.5 g in 1 package, 76725-012-02 100 package in 1 canister / 2.5 g in 1 package. 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 Dr Clinic 75% Alcohol Wipes?

• Open container plastic cover, Tear off moisture seal film. Pull out wipe corner from the center of wipe roll; twist wipe corner through the dispensing center of the canister. Next sheets pop up automatically. Keep center cap closed to prevent moisture loss.• No need to rinse after usage. Allow skin to dry without wiping. For adults and children 2 years and over. Discard properly after use. Supervise children under 6 years of age when using this product to avoid swallowing.

Which are Dr Clinic 75% Alcohol Wipes UNII Codes?

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

Which are Dr Clinic 75% Alcohol Wipes 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".