NDC 0311-0704 Almay Wake-up Liquid Make-up
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0311 - Almay, Inc.
- 0311-0704 - Almay Wake-up Liquid Make-up
Product Packages
NDC Code 0311-0704-01
Package Description: 30 mL in 1 TUBE
Product Details
What is NDC 0311-0704?
What are the uses for Almay Wake-up Liquid Make-up?
Which are Almay Wake-up Liquid Make-up UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Almay Wake-up Liquid Make-up 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:
- WATER (UNII: 059QF0KO0R)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- C13-16 ISOPARAFFIN (UNII: LED42LZG6O)
- NYLON-12 (UNII: 446U8J075B)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- ISOCETYL STEARATE (UNII: 3RJ7186O9W)
- ISOTRIDECYL ISONONANOATE (UNII: WEF51750MT)
- TROMETHAMINE (UNII: 023C2WHX2V)
- PENTAERYTHRITYL TETRAISOSTEARATE (UNII: 9D7IK5483F)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- CUCUMBER (UNII: YY7C30VXJT)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- COCONUT (UNII: 3RT3536DHY)
- CAFFEINE (UNII: 3G6A5W338E)
- STEARETH-2 (UNII: V56DFE46J5)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- PROPYLENE GLYCOL LAURATES (UNII: 40KT317HGP)
- PROPYLENE GLYCOL STEARATE (UNII: MZM1I680W0)
- PEG-10 SORBITAN LAURATE (UNII: 4Z93U4C2WN)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- LAURETH-7 (UNII: Z95S6G8201)
- XANTHAN GUM (UNII: TTV12P4NEE)
- METHICONE (20 CST) (UNII: 6777U11MKT)
- STEARETH-21 (UNII: 53J3F32P58)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
* 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".