NDC 73166-107 Skin Aid Medics Antibacterial Cucumber Melon Gentle
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What is NDC 73166-107?
What are the uses for Skin Aid Medics Antibacterial Cucumber Melon Gentle?
Which are Skin Aid Medics Antibacterial Cucumber Melon Gentle UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Skin Aid Medics Antibacterial Cucumber Melon Gentle 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- MAGNESIUM NITRATE (UNII: 77CBG3UN78)
- MAGNESIUM CHLORIDE ANHYDROUS (UNII: 59XN63C8VM)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYETHYLENE GLYCOL 100000 (UNII: V46Y6OJ5QB)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- WATER (UNII: 059QF0KO0R)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
What is the NDC to RxNorm Crosswalk for Skin Aid Medics Antibacterial Cucumber Melon Gentle?
- 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".