NDC 51774-008 Professional

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:
51774-008
Proprietary Name:
Professional
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]
08-24-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 51774-008-02

Package Description: 60 mL in 1 BOTTLE

NDC Code 51774-008-04

Package Description: 120 mL in 1 BOTTLE

NDC Code 51774-008-05

Package Description: 125 mL in 1 BOTTLE

NDC Code 51774-008-12

Package Description: 360 mL in 1 BOTTLE

NDC Code 51774-008-16

Package Description: 480 mL in 1 BOTTLE

NDC Code 51774-008-28

Package Description: 3840 mL in 1 BOTTLE

NDC Code 51774-008-32

Package Description: 960 mL in 1 BOTTLE

Product Details

What is NDC 51774-008?

The NDC code 51774-008 is assigned by the FDA to the product Professional which is product labeled by Industrias Chamer S.a. De C.v.. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 51774-008-02 60 ml in 1 bottle , 51774-008-04 120 ml in 1 bottle , 51774-008-05 125 ml in 1 bottle , 51774-008-12 360 ml in 1 bottle , 51774-008-16 480 ml in 1 bottle , 51774-008-28 3840 ml in 1 bottle , 51774-008-32 960 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 Professional?

Clean the affected area.Spray a small amount of this product on the area 1 to 3 times daily.May be covered with sterile bandage.If bandaged, let dry first.

Which are Professional UNII Codes?

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

Which are Professional 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 Professional?

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:

* Please review the disclaimer below.

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".