NDC 36800-109 Topcare Antibacterial Foaming Hand Fresh Pear
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 36800-109?
What are the uses for Topcare Antibacterial Foaming Hand Fresh Pear?
Which are Topcare Antibacterial Foaming Hand Fresh Pear UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Topcare Antibacterial Foaming Hand Fresh Pear 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)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- GLYCERIN (UNII: PDC6A3C0OX)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- HYDROXYETHYL CELLULOSE (5000 CPS AT 1%) (UNII: X70SE62ZAR)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE SODIUM (UNII: MP1J8420LU)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
What is the NDC to RxNorm Crosswalk for Topcare Antibacterial Foaming Hand Fresh Pear?
- RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap
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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".