NDC 77046-100 Hand Sanitizing Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77046 - Zhejiang Huashun Technology Co.,ltd
- 77046-100 - Hand Sanitizing Wipes
Product Packages
NDC Code 77046-100-03
Package Description: 100 PATCH in 1 BOX / 4 g in 1 PATCH
NDC Code 77046-100-04
Package Description: 3 BAG in 1 BOX / 30 PATCH in 1 BAG / 4.45 g in 1 PATCH
Product Details
What is NDC 77046-100?
What are the uses for Hand Sanitizing Wipes?
Which are Hand Sanitizing Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) (Active Moiety)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) (Active Moiety)
- BRONOPOL (UNII: 6PU1E16C9W)
- BRONOPOL (UNII: 6PU1E16C9W) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Hand 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:
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- WATER (UNII: 059QF0KO0R)
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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".