NDC 58466-033 Nanocare Moisturizing Sunscreen Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58466 - Deramzone Solutions, Inc.
- 58466-033 - Nanocare
Product Packages
NDC Code 58466-033-33
Package Description: 1 BOTTLE in 1 CARTON / 88 mL in 1 BOTTLE
Product Details
What is NDC 58466-033?
What are the uses for Nanocare Moisturizing Sunscreen Spf 50?
Which are Nanocare Moisturizing Sunscreen Spf 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOPHENONE (UNII: 701M4TTV9O)
- BENZOPHENONE (UNII: 701M4TTV9O) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Nanocare Moisturizing Sunscreen Spf 50 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)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- ALCOHOL (UNII: 3K9958V90M)
- DIOCTYL MALEATE (UNII: OD88G8439L)
- SORBITOL (UNII: 506T60A25R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TROLAMINE (UNII: 9O3K93S3TK)
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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".