NDC 75757-101 Cyber Clean Power Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75757 - Joker Ag
- 75757-101 - Cyber Clean Power Gel
Product Packages
NDC Code 75757-101-01
Package Description: 30 mL in 1 BOTTLE
NDC Code 75757-101-02
Package Description: 43 mL in 1 BOTTLE
NDC Code 75757-101-03
Package Description: 60 mL in 1 BOTTLE
NDC Code 75757-101-04
Package Description: 100 mL in 1 BOTTLE
NDC Code 75757-101-05
Package Description: 220 mL in 1 BOTTLE
NDC Code 75757-101-06
Package Description: 300 mL in 1 BOTTLE
NDC Code 75757-101-07
Package Description: 500 mL in 1 BOTTLE
NDC Code 75757-101-08
Package Description: 995 mL in 1 BOTTLE
NDC Code 75757-101-09
Package Description: 1890 mL in 1 BOTTLE
NDC Code 75757-101-10
Package Description: 2000 mL in 1 BOTTLE
Product Details
What is NDC 75757-101?
What are the uses for Cyber Clean Power Gel?
Which are Cyber Clean Power Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Cyber Clean Power Gel 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
- TRIISOPROPANOLAMINE (UNII: W9EN9DLM98)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Cyber Clean Power Gel?
- RxCUI: 2277550 - ethanol 72 % Topical Gel
- RxCUI: 2277550 - ethanol 0.72 ML/ML Topical Gel
* Please review the disclaimer below.
[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".