NDC 59614-511 Sun Protection Body Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59614 - Juvena Produits De Beaute Gmbh
- 59614-511 - Sun Protection Body
Product Packages
NDC Code 59614-511-02
Package Description: 1 BOTTLE in 1 BOX / 180 mL in 1 BOTTLE (59614-511-01)
NDC Code 59614-511-11
Package Description: .09 mL in 1 DRUM
Product Details
What is NDC 59614-511?
What are the uses for Sun Protection Body Spf 30?
Which are Sun Protection Body Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Sun Protection Body Spf 30 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:
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALLANTOIN (UNII: 344S277G0Z)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- LAURETH-7 (UNII: Z95S6G8201)
- METHYLPARABEN (UNII: A2I8C7HI9T)
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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".