NDC 58443-0219 Australian Gold Hello Kitty Mineral Faces Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 58443-0219?
What are the uses for Australian Gold Hello Kitty Mineral Faces Sunscreen?
Which are Australian Gold Hello Kitty Mineral Faces Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Australian Gold Hello Kitty Mineral Faces Sunscreen 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:
- POLYGLYCERYL-3 DISTEARATE (UNII: ZI1LK470XV)
- XANTHAN GUM (UNII: TTV12P4NEE)
- BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CETEARETH-22 (UNII: 28VZG1E234)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TRIMETHYLSILOXYSILICATE (M/Q 0.8-1.0) (UNII: 25LXE464L2)
- GLYCERIN (UNII: PDC6A3C0OX)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- METHYLCELLULOSE (100 CPS) (UNII: 4GFU244C4J)
- WATER (UNII: 059QF0KO0R)
- PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- BUDDLEJA DAVIDII LEAF (UNII: X380815D32)
- ARTEMISIA PRINCEPS LEAF OIL (UNII: F9S1101A2V)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- DIBUTYL ADIPATE (UNII: F4K100DXP3)
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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".