NDC 74773-0027 Kundal Pure And Safe Sanitizing Tissue (benzalkonium Chloride)
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 74773-0027?
What are the uses for Kundal Pure And Safe Sanitizing Tissue (benzalkonium Chloride)?
Which are Kundal Pure And Safe Sanitizing Tissue (benzalkonium Chloride) UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Kundal Pure And Safe Sanitizing Tissue (benzalkonium Chloride) 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:
- COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- WATER (UNII: 059QF0KO0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
What is the NDC to RxNorm Crosswalk for Kundal Pure And Safe Sanitizing Tissue (benzalkonium Chloride)?
- RxCUI: 1038856 - benzalkonium Cl 0.1 % Medicated Pad
- RxCUI: 1038856 - benzalkonium chloride 1 MG/ML Medicated Pad
- RxCUI: 1038856 - benzalkonium chloride 0.1 % Medicated Wipes
- RxCUI: 1038856 - benzalkonium chloride 0.1 % 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".