NDC 80991-003 Sanitizing Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 80991 - Zhejiang Fanjia Medical Equipment Co., Ltd.
- 80991-003 - Sanitizing Wipes
Product Packages
NDC Code 80991-003-04
Package Description: 160 APPLICATOR in 1 CANISTER / 5 g in 1 APPLICATOR
Product Details
What is NDC 80991-003?
What are the uses for Sanitizing Wipes?
Which are Sanitizing Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Sanitizing 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:
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- WATER (UNII: 059QF0KO0R)
- FAGRAEA BERTEROANA FLOWER OIL (UNII: 6665W245VP)
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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".