NDC 71611-068 Antibacterial Handwash Lavender Bouquet
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71611 - Click Products Llc
- 71611-068 - Antibacterial Handwash
Product Packages
NDC Code 71611-068-01
Package Description: 400 mL in 1 BOTTLE
NDC Code 71611-068-02
Package Description: 2000 mL in 1 BOTTLE
Product Details
What is NDC 71611-068?
What are the uses for Antibacterial Handwash Lavender Bouquet?
Which are Antibacterial Handwash Lavender Bouquet UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Antibacterial Handwash Lavender Bouquet 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:
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- MAGNESIUM CITRATE (UNII: RHO26O1T9V)
- GLYCERIN (UNII: PDC6A3C0OX)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- SULISOBENZONE (UNII: 1W6L629B4K)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
What is the NDC to RxNorm Crosswalk for Antibacterial Handwash Lavender Bouquet?
- 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".