NDC 77720-009 Hand Sanitizing Wipes
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 77720-009?
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:
- 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:
- WATER (UNII: 059QF0KO0R)
- QUATERNIUM-52 (UNII: 588EQF3H1P)
- PEG-75 LANOLIN (UNII: 09179OX7TB)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
- PEG-8 DIMETHICONE (UNII: GIA7T764OD)
- DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- CHAMOMILE (UNII: FGL3685T2X)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
What is the NDC to RxNorm Crosswalk for Hand Sanitizing Wipes?
- RxCUI: 1812737 - benzalkonium Cl 0.3 % Medicated Pad
- RxCUI: 1812737 - benzalkonium chloride 3 MG/ML Medicated Pad
- RxCUI: 1812737 - benzalkonium chloride 0.3 % Medicated Wipe
- RxCUI: 1812737 - benzalkonium chloride 0.3 % Topical Cloth
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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".