NDC 72645-003 Cocooil Spf50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72645 - Cocooil Limited
- 72645-003 - Cocooil Spf50
Product Packages
NDC Code 72645-003-01
Package Description: 100 mL in 1 BOTTLE
NDC Code 72645-003-02
Package Description: 200 mL in 1 BOTTLE
Product Details
What is NDC 72645-003?
What are the uses for Cocooil Spf50?
Which are Cocooil Spf50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Cocooil Spf50 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:
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- TRICONTANYL POVIDONE (UNII: N0SS3Q238D)
- TOCOPHEROL (UNII: R0ZB2556P8)
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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".