NDC 61995-0020 J0832014 Jason Sun Sport Sunscreen Spf45
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61995 - The Hain Celestial Group, Inc.
- 61995-0020 - J0832014 Jason Sun Sport Sunscreen Spf45
Product Packages
NDC Code 61995-0020-4
Package Description: 113 g in 1 TUBE
Product Details
What is NDC 61995-0020?
What are the uses for J0832014 Jason Sun Sport Sunscreen Spf45?
Which are J0832014 Jason Sun Sport Sunscreen Spf45 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (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 J0832014 Jason Sun Sport Sunscreen Spf45 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:
- ACAI (UNII: 46AM2VJ0AW)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- ORANGE OIL (UNII: AKN3KSD11B)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CANANGA OIL (UNII: 8YOY78GNNX)
* 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".