NDC 24653-271 Cc Cream Medium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 24653 - Janssen Cosmetics Gmbh
- 24653-271 - Cc Cream Medium
Product Packages
NDC Code 24653-271-02
Package Description: 1 BOTTLE, PUMP in 1 BOX / 30 mL in 1 BOTTLE, PUMP (24653-271-01)
Product Details
What is NDC 24653-271?
Which are Cc Cream Medium UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Cc Cream Medium 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)
- PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PEG-20 METHYL GLUCOSE SESQUISTEARATE (UNII: 0345752X7U)
- SODIUM ALUMINIUM SILICATE (UNII: 058TS43PSM)
- STEARETH-21 (UNII: 53J3F32P58)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- LAUROYL LYSINE (UNII: 113171Q70B)
- ISODON RUBESCENS TOP (UNII: 03NNJ0PH79)
- CULTIVATED MUSHROOM (UNII: 54C8E6W6JY)
- HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
- YEAST (UNII: 3NY3SM6B8U)
- SOY ISOFLAVONES (UNII: 71B37NR06D)
- GARDEN CRESS SPROUT (UNII: PWQ18YNR62)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LEVULINATE (UNII: VK44E1MQU8)
- LEVULINIC ACID (UNII: RYX5QG61EI)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TOCOPHEROL (UNII: R0ZB2556P8)
- MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)
- ALCOHOL (UNII: 3K9958V90M)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
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[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".