NDC 58892-336 Solar Protection Formula Tizo2 Light Skin Formula Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58892 - Fallien Cosmeceuticals, Ltd.
- 58892-336 - Solar Protection Formula Tizo2 Light Skin Formula
Product Packages
NDC Code 58892-336-45
Package Description: 1 TUBE in 1 CARTON / 44.4 mL in 1 TUBE
NDC Code 58892-336-50
Package Description: 1 TUBE in 1 CARTON / 50 mL in 1 TUBE
Product Details
What is NDC 58892-336?
What are the uses for Solar Protection Formula Tizo2 Light Skin Formula Sunscreen?
Which are Solar Protection Formula Tizo2 Light Skin Formula 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 Solar Protection Formula Tizo2 Light Skin Formula 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:
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE 20 (UNII: H8YMB5QY0D)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- DIMETHICONOL (2000 CST) (UNII: T74O12AN6Y)
- LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX)
- HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
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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".