NDC 17630-2010 Banana Boat Baby Sin Lagrimas Spf 50 Pump
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 17630-2010?
Which are Banana Boat Baby Sin Lagrimas Spf 50 Pump UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Banana Boat Baby Sin Lagrimas Spf 50 Pump 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:
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- GLUCOSE OXIDASE (UNII: 0T8392U5N1)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
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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".