NDC 75449-1001 Gastrodia Elata Peptide Hand Sanitizing

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:
75449-1001
Proprietary Name:
Gastrodia Elata Peptide Hand Sanitizing
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
75449
Start Marketing Date: [9]
04-24-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 75449-1001?

The NDC code 75449-1001 is assigned by the FDA to the product Gastrodia Elata Peptide Hand Sanitizing which is product labeled by Tonghua Ren-sheng-yuan Biotechnology Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75449-1001-1 500 ml in 1 bottle . 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 Gastrodia Elata Peptide Hand Sanitizing?

1.Sanitary hand disinfection: Take the right amount of this product on the palm, both hands rub each other to make uniform coating on each part for 1 minute. 2. Surgical hand antisepsis: After surgical hand washing, apply proper amount of this product evenly to the skin of the forearm and the lower third of the upper arm of both hands and rub for 3 to 5 minutes until dry.

Which are Gastrodia Elata Peptide Hand Sanitizing UNII Codes?

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

Which are Gastrodia Elata Peptide Hand Sanitizing 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".