NDC 10157-8009 Fruit Smoothies
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10157 - Blistex Inc.
- 10157-8009 - Fruit Smoothies
Product Characteristics
GREEN (C48329)
PINK (C48328)
Product Packages
NDC Code 10157-8009-1
Package Description: 1 KIT in 1 BLISTER PACK * 2.83 g in 1 CYLINDER * 2.83 g in 1 CYLINDER * 2.83 g in 1 CYLINDER
Product Details
What is NDC 10157-8009?
What are the uses for Fruit Smoothies?
Which are Fruit Smoothies UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Fruit Smoothies 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:
- ALUMINUM OXIDE (UNII: LMI26O6933)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- DIETHYLHEXYL ADIPATE (UNII: MBY1SL921L)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- ISOPROPYL STEARATE (UNII: 43253ZW1MZ)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- SACCHARIN (UNII: FST467XS7D)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
* 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".