NDC 51523-102 Natural Sun Aq Total Anti-aging Essence Sun
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51523 - Thefaceshop Co., Ltd
- 51523-102 - Natural Sun Aq Total Anti-aging Essence Sun
Product Packages
NDC Code 51523-102-02
Package Description: 1 CONTAINER in 1 BOX / 50 mL in 1 CONTAINER (51523-102-01)
Product Details
What is NDC 51523-102?
What are the uses for Natural Sun Aq Total Anti-aging Essence Sun?
Which are Natural Sun Aq Total Anti-aging Essence Sun UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- ENZACAMENE (UNII: 8I3XWY40L9)
- ENZACAMENE (UNII: 8I3XWY40L9) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
Which are Natural Sun Aq Total Anti-aging Essence Sun 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 (UNII: NMQ347994Z)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- POLYOXYL 100 STEARATE (UNII: YD01N1999R)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- XANTHAN GUM (UNII: TTV12P4NEE)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- BENZYL BENZOATE (UNII: N863NB338G)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- TROLAMINE (UNII: 9O3K93S3TK)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- GLYCOL STEARATE (UNII: 0324G66D0E)
- MINERAL OIL (UNII: T5L8T28FGP)
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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".