NDC 20151-069 Cleanser Balancing
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 20151 - Casmara Cosmetics, Sa
- 20151-069 - Cleanser Balancing
Product Packages
NDC Code 20151-069-02
Package Description: 1 BOTTLE, DISPENSING in 1 BOTTLE, DISPENSING / 150 mL in 1 BOTTLE, DISPENSING (20151-069-01)
Product Details
What is NDC 20151-069?
What are the uses for Cleanser Balancing?
Which are Cleanser Balancing UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are Cleanser Balancing 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:
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SORBIC ACID (UNII: X045WJ989B)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- WATER (UNII: 059QF0KO0R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- PERFLUNAFENE (UNII: 54A06VV62N)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- LYCIUM BARBARUM FRUIT (UNII: 930626MWDL)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- LINALOOL, (+)- (UNII: F4VNO44C09)
* 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".