NDC 51774-009 Jetclean

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:
51774-009
Proprietary Name:
Jetclean
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Industrias Chamer S.a. De C.v.
Labeler Code:
51774
Start Marketing Date: [9]
09-15-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 51774-009-16

Package Description: 480 mL in 1 BOTTLE

NDC Code 51774-009-24

Package Description: 720 mL in 1 BOTTLE

NDC Code 51774-009-32

Package Description: 960 mL in 1 BOTTLE

Product Details

What is NDC 51774-009?

The NDC code 51774-009 is assigned by the FDA to the product Jetclean which is product labeled by Industrias Chamer S.a. De C.v.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 51774-009-16 480 ml in 1 bottle , 51774-009-24 720 ml in 1 bottle , 51774-009-32 960 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 Jetclean?

Apply to hands, skin or any surface twice daily or as often as desired. Not recommended for wood as it could stain. Don't spray on or near flame. Avoid contact with eyes. Not for consumption.

Which are Jetclean UNII Codes?

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

Which are Jetclean 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 Jetclean?

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".