NDC 70281-338 Bullfrog Spf50 Land Sport Quik
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70281 - Solskyn Personal Care Llc
- 70281-338 - Bullfrog Spf50 Land Sport Quik
Product Packages
NDC Code 70281-338-13
Package Description: 147 mg in 1 BOTTLE
Product Details
What is NDC 70281-338?
What are the uses for Bullfrog Spf50 Land Sport Quik?
Which are Bullfrog Spf50 Land Sport Quik UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Bullfrog Spf50 Land Sport Quik 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:
- VACHELLIA FARNESIANA FLOWER (UNII: 8487B3MG6D)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- PHENETHYL BENZOATE (UNII: 0C143929GK)
- PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ROSEMARY (UNII: IJ67X351P9)
- ALCOHOL (UNII: 3K9958V90M)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
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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".