NDC 61995-2020 Sport Sunscreen Spf 45
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 61995-2020?
What are the uses for Sport Sunscreen Spf 45?
Which are Sport Sunscreen Spf 45 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)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Sport Sunscreen Spf 45 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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERIN (UNII: PDC6A3C0OX)
- VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- MATRICARIA CHAMOMILLA FLOWERING TOP (UNII: 3VNC7T6Z02)
- GINKGO (UNII: 19FUJ2C58T)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- WATER (UNII: 059QF0KO0R)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ALCOHOL (UNII: 3K9958V90M)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
* Please review the disclaimer below.
[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".