NDC 62382-0324 Chg
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 62382-0324-0
Package Description: 3 mL in 1 POUCH
NDC Code 62382-0324-1
Package Description: .2 mL in 1 POUCH
NDC Code 62382-0324-2
Package Description: .3 mL in 1 POUCH
NDC Code 62382-0324-3
Package Description: .4 mL in 1 POUCH
NDC Code 62382-0324-4
Package Description: .5 mL in 1 POUCH
NDC Code 62382-0324-5
Package Description: .6 mL in 1 POUCH
NDC Code 62382-0324-6
Package Description: .67 mL in 1 POUCH
NDC Code 62382-0324-7
Package Description: 1 mL in 1 POUCH
NDC Code 62382-0324-8
Package Description: 1.5 mL in 1 POUCH
NDC Code 62382-0324-9
Package Description: 1.75 mL in 1 POUCH
Product Details
What is NDC 62382-0324?
What are the uses for Chg?
Which are Chg UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
Which are Chg 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:
- WATER (UNII: 059QF0KO0R)
- CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
What is the NDC to RxNorm Crosswalk for Chg?
- RxCUI: 797544 - isopropyl alcohol 70 % Medicated Pad
- RxCUI: 797544 - isopropyl alcohol 0.7 ML/ML Medicated Pad
- RxCUI: 797544 - isopropyl alcohol 70 % Topical Cloth
- RxCUI: 797544 - isopropyl alcohol 70 % Topical Swab
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[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".