NDC 70493-429 Premium Age Protector
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 70493-429?
Which are Premium Age Protector UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Premium Age Protector 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:
- SIGESBECKIA ORIENTALIS FLOWERING TOP (UNII: 6UL878YAR7)
- POTASSIUM ALUMINUM DISILICATE (UNII: SRB14JRX6C)
- STEARETH-21 (UNII: 53J3F32P58)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ALCOHOL (UNII: 3K9958V90M)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)
- YEAST (UNII: 3NY3SM6B8U)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SOY ISOFLAVONES (UNII: 71B37NR06D)
- GARDEN CRESS SPROUT (UNII: PWQ18YNR62)
- WATER (UNII: 059QF0KO0R)
- METHYL GLUCOSE SESQUISTEARATE (UNII: V1YW10H14D)
- ISODON RUBESCENS TOP (UNII: 03NNJ0PH79)
- LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
- LEVULINIC ACID (UNII: RYX5QG61EI)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- TOCOPHEROL (UNII: R0ZB2556P8)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- METHYL BENZOATE (UNII: 6618K1VJ9T)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4)
- SODIUM LEVULINATE (UNII: VK44E1MQU8)
* 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".