NDC 78122-030 Anti-bacterial Multi-purpose Cleaning Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78122 - Wenzhou Guanshang Paper Co., Ltd
- 78122-030 - Anti-bacterial Multi-purpose Cleaning Wipes
Product Characteristics
Product Packages
NDC Code 78122-030-30
Package Description: 30 CLOTH in 1 PACKAGE
Product Details
What is NDC 78122-030?
What are the uses for Anti-bacterial Multi-purpose Cleaning Wipes?
Which are Anti-bacterial Multi-purpose Cleaning Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
- BRONOPOL (UNII: 6PU1E16C9W)
- BRONOPOL (UNII: 6PU1E16C9W) (Active Moiety)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) (Active Moiety)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) (Active Moiety)
Which are Anti-bacterial Multi-purpose Cleaning Wipes 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:
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
* 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".