NDC 76098-002 The Green Beaver Company Spf 40 Kids Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 76098-002?
Which are The Green Beaver Company Spf 40 Kids Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are The Green Beaver Company Spf 40 Kids 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:
- CEROTIC ACID (UNII: D42CQN6P36)
- HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
- SQUALENE (UNII: 7QWM220FJH)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
- TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- SODIUM BETA-SITOSTERYL SULFATE (UNII: I289C8TPSV)
- LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
- WATER (UNII: 059QF0KO0R)
- KARUM SEED OIL (UNII: 62160PU6FJ)
- HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- RUBUS IDAEUS FRUIT VOLATILE OIL (UNII: 276X2YNL0K)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- ISOSTEARIC ACID (UNII: X33R8U0062)
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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".