NDC 71995-000 Advantage Sanitizing 900 Wipes Per Roll
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71995 - 2xl Corporation
- 71995-000 - Advantage Sanitizing 900 Wipes Per Roll
Product Packages
NDC Code 71995-000-00
Package Description: 900 PATCH in 1 POUCH / 5 mL in 1 PATCH
Product Details
What is NDC 71995-000?
What are the uses for Advantage Sanitizing 900 Wipes Per Roll?
Which are Advantage Sanitizing 900 Wipes Per Roll UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Advantage Sanitizing 900 Wipes Per Roll 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)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- GLYCERIN (UNII: PDC6A3C0OX)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
What is the NDC to RxNorm Crosswalk for Advantage Sanitizing 900 Wipes Per Roll?
- RxCUI: 1038741 - benzalkonium Cl 0.12 % Medicated Pad
- RxCUI: 1038741 - benzalkonium chloride 1.2 MG/ML Medicated Pad
- RxCUI: 1038741 - benzalkonium chloride 0.12 % Medicated Wipe
- RxCUI: 1038741 - benzalkonium chloride 0.12 % Topical Cloth
- RxCUI: 1038741 - benzalkonium chloride 0.12 % Topical Swab
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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".