NDC 80138-201 Bacteria Zero Premium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 80138 - Kumsung Enc Co., Ltd
- 80138-201 - Bacteria Zero Premium
Product Packages
NDC Code 80138-201-01
Package Description: 60 mL in 1 BOTTLE, SPRAY
NDC Code 80138-201-02
Package Description: 100 mL in 1 BOTTLE, SPRAY
NDC Code 80138-201-03
Package Description: 500 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 80138-201?
What are the uses for Bacteria Zero Premium?
Which are Bacteria Zero Premium UNII Codes?
The UNII codes for the active ingredients in this product are:
- PERACETIC ACID (UNII: I6KPI2E1HD)
- PERACETIC ACID (UNII: I6KPI2E1HD) (Active Moiety)
Which are Bacteria Zero Premium 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:
- ACETIC ACID (UNII: Q40Q9N063P)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- PHOSPHOROUS ACID (UNII: 35V6A8JW8E)
- WATER (UNII: 059QF0KO0R)
* 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".