NDC 49203-740 Skin Doctors Photo Age Reverse
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 49203-740?
What are the uses for Skin Doctors Photo Age Reverse?
Which are Skin Doctors Photo Age Reverse UNII Codes?
The UNII codes for the active ingredients in this product are:
- THERMUS THERMOPHILUS LYSATE (UNII: 775R692494)
- THERMUS THERMOPHILUS LYSATE (UNII: 775R692494) (Active Moiety)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are Skin Doctors Photo Age Reverse 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)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PEG-20 STEARATE (UNII: NBX892EA57)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DIMETHICONE 200 (UNII: RGS4T2AS00)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
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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".