NDC 42248-131 Perfect Bust Body
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42248 - Zenith Medicosm Sl
- 42248-131 - Perfect Bust
Product Packages
NDC Code 42248-131-01
Package Description: 150 mL in 1 BOTTLE
Product Details
What is NDC 42248-131?
Which are Perfect Bust Body UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Perfect Bust Body 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:
- PEG-2 STEARATE (UNII: 94YQ11Y95F)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- WATER (UNII: 059QF0KO0R)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE (UNII: KBC00G95HI)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SOY PROTEIN (UNII: R44IWB3RN5)
- SHEA BUTTER (UNII: K49155WL9Y)
- LAMINARIA DIGITATA (UNII: 15E7C67EE8)
- HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
- MINERAL OIL (UNII: T5L8T28FGP)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GERANIOL (UNII: L837108USY)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- ALLANTOIN (UNII: 344S277G0Z)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)
- EDETIC ACID (UNII: 9G34HU7RV0)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BOMBYX MORI FIBER (UNII: 6LK42KUV6W)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
* 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".