NDC 75862-011 Birds Garden Lip Balm Dark Eyed Junco Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 75862-011?
Which are Birds Garden Lip Balm Dark Eyed Junco Spf 30 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)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Birds Garden Lip Balm Dark Eyed Junco 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:
- PETROLATUM (UNII: 4T6H12BN9U)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- PARAFFIN (UNII: I9O0E3H2ZE)
- CANDELILLA WAX (UNII: WL0328HX19)
- LOW DENSITY POLYETHYLENE (UNII: J245LN42AI)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- LANOLIN (UNII: 7EV65EAW6H)
- OLEYL ALCOHOL (UNII: 172F2WN8DV)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SOYBEAN OIL (UNII: 241ATL177A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SACCHARIN (UNII: FST467XS7D)
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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".