NDC 79294-001 Antiseptic Sanitizing Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79294 - Hangzhou Wipex Nonwovens Co., Ltd.
- 79294-001 - Antiseptic Sanitizing Wipes
Product Packages
NDC Code 79294-001-01
Package Description: 160 BAG in 1 CARTON / 10 NOT APPLICABLE in 1 BAG / 60 g in 1 NOT APPLICABLE
NDC Code 79294-001-02
Package Description: 4 BAG in 1 CARTON / 1200 NOT APPLICABLE in 1 BAG / 4700 g in 1 NOT APPLICABLE
NDC Code 79294-001-03
Package Description: 48 BAG in 1 CARTON / 50 NOT APPLICABLE in 1 BAG / 237 g in 1 NOT APPLICABLE
NDC Code 79294-001-04
Package Description: 24 CANISTER in 1 CARTON / 80 NOT APPLICABLE in 1 CANISTER / 337 g in 1 NOT APPLICABLE
NDC Code 79294-001-05
Package Description: 24 CANISTER in 1 CARTON / 100 NOT APPLICABLE in 1 CANISTER / 540 g in 1 NOT APPLICABLE
NDC Code 79294-001-06
Package Description: 12 CANISTER in 1 CARTON / 180 NOT APPLICABLE in 1 CANISTER / 1120 g in 1 NOT APPLICABLE
NDC Code 79294-001-07
Package Description: 12 CANISTER in 1 CARTON / 220 NOT APPLICABLE in 1 CANISTER / 450 g in 1 NOT APPLICABLE
NDC Code 79294-001-08
Package Description: 4 BAG in 1 CARTON / 800 NOT APPLICABLE in 1 BAG / 1638 g in 1 NOT APPLICABLE
NDC Code 79294-001-09
Package Description: 4 BAG in 1 CARTON / 900 NOT APPLICABLE in 1 BAG / 1842 g in 1 NOT APPLICABLE
NDC Code 79294-001-10
Package Description: 4 BAG in 1 CARTON / 1500 NOT APPLICABLE in 1 BAG / 3071 g in 1 NOT APPLICABLE
Product Details
What is NDC 79294-001?
What are the uses for Antiseptic Sanitizing Wipes?
Which are Antiseptic 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 Antiseptic 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:
- WATER (UNII: 059QF0KO0R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
- MENTHOL (UNII: L7T10EIP3A)
- TEA TREE OIL (UNII: VIF565UC2G)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
What is the NDC to RxNorm Crosswalk for Antiseptic Sanitizing Wipes?
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 1.3 MG/ML Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Topical Swab
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Swab
* 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".