NDC 58443-0362 Derma Swiss Spf 50 Mineral
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58443 - Prime Enterprises Inc.
- 58443-0362 - Derma Swiss
Product Characteristics
Product Packages
NDC Code 58443-0362-3
Package Description: 89 mL in 1 TUBE
Product Details
What is NDC 58443-0362?
What are the uses for Derma Swiss Spf 50 Mineral?
Which are Derma Swiss Spf 50 Mineral 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 Derma Swiss Spf 50 Mineral 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:
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALLANTOIN (UNII: 344S277G0Z)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- SHEA BUTTER (UNII: K49155WL9Y)
- WATER (UNII: 059QF0KO0R)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- GLYCERIN (UNII: PDC6A3C0OX)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- LEVOMENOL (UNII: 24WE03BX2T)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PANTHENOL (UNII: WV9CM0O67Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALUMINUM OXIDE (UNII: LMI26O6933)
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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".