NDC 53208-478 Isaknox Ageless Serum Moist Pearl Base
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53208 - Lg Household And Healthcare, Inc.
- 53208-478 - Isaknox Ageless Serum Moist Pearl Base
Product Packages
NDC Code 53208-478-02
Package Description: 1 CONTAINER in 1 BOX / 40 mL in 1 CONTAINER (53208-478-01)
Product Details
What is NDC 53208-478?
Which are Isaknox Ageless Serum Moist Pearl Base 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (Active Moiety)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- STEARIC ACID (UNII: 4ELV7Z65AP) (Active Moiety)
- HYDROXYPROLINE (UNII: RMB44WO89X)
- HYDROXYPROLINE (UNII: RMB44WO89X) (Active Moiety)
Which are Isaknox Ageless Serum Moist Pearl Base 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- ISODODECANE (UNII: A8289P68Y2)
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- SORBITAN (UNII: 6O92ICV9RU)
- HECTORITE (UNII: 08X4KI73EZ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
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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".