NDC 61481-3004 Kinesys Broad Spectrum Spf 30 Girl Alcohol-free Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61481 - Wilc Healthcare Inc
- 61481-3004 - Kinesys
Product Packages
NDC Code 61481-3004-1
Package Description: 30 mL in 1 BOTTLE, SPRAY
NDC Code 61481-3004-4
Package Description: 120 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 61481-3004?
What are the uses for Kinesys Broad Spectrum Spf 30 Girl Alcohol-free Sunscreen?
Which are Kinesys Broad Spectrum Spf 30 Girl Alcohol-free Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Kinesys Broad Spectrum Spf 30 Girl Alcohol-free 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:
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- DIPHENYLSILOXY PHENYL TRIMETHICONE (UNII: I445L28B12)
- VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
- TOCOPHEROL (UNII: R0ZB2556P8)
- LEVOMENOL (UNII: 24WE03BX2T)
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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".