NDC 58443-0319 Austalian Gold Broad Spectrum Spf 50 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 58443-0319?
What are the uses for Austalian Gold Broad Spectrum Spf 50 Sunscreen?
Which are Austalian Gold Broad Spectrum Spf 50 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Austalian Gold Broad Spectrum Spf 50 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:
- PANTHENOL (UNII: WV9CM0O67Z)
- FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SQUALANE (UNII: GW89575KF9)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- PORPHYRA UMBILICALIS (UNII: 14AN0J70WO)
- GLYCERIN (UNII: PDC6A3C0OX)
- KAKADU PLUM (UNII: 0ZQ1D2FDLI)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- SHEA BUTTER (UNII: K49155WL9Y)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
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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".