NDC 76665-025 Fundamentals Handlotion
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76665 - Clean Beauty Concepts
- 76665-025 - Fundamentals Handlotion
Product Packages
NDC Code 76665-025-01
Package Description: 3785 mL in 1 BOTTLE, DISPENSING
NDC Code 76665-025-02
Package Description: 60 mL in 1 BOTTLE, DISPENSING
NDC Code 76665-025-08
Package Description: 236 mL in 1 BOTTLE, DISPENSING
NDC Code 76665-025-16
Package Description: 473 mL in 1 BOTTLE, DISPENSING
Product Details
What is NDC 76665-025?
What are the uses for Fundamentals Handlotion?
Which are Fundamentals Handlotion UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Fundamentals Handlotion 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:
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BASIL (UNII: 2U0KZP0FDW)
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PETROLATUM (UNII: 4T6H12BN9U)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SODIUM ACRYLATE (UNII: 7C98FKB43H)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- BASIL OIL (UNII: Z129UMU8LE)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- CARBOMER 1342 (UNII: 809Y72KV36)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- C12-20 ALKYL BENZOATE (UNII: Y15I6XI14C)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
* Please review the disclaimer below.
[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".