NDC 50184-1032 Hope In A Jar Broad Spectrum Spf 25 Sunscreen And Moisturizer For All Skin Types
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 50184-1032?
What are the uses for Hope In A Jar Broad Spectrum Spf 25 Sunscreen And Moisturizer For All Skin Types?
Which are Hope In A Jar Broad Spectrum Spf 25 Sunscreen And Moisturizer For All Skin Types 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 Hope In A Jar Broad Spectrum Spf 25 Sunscreen And Moisturizer For All Skin Types 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:
- WATER (UNII: 059QF0KO0R)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- DIBUTYL ADIPATE (UNII: F4K100DXP3)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- LAURYL LACTATE (UNII: G5SU0BFK7O)
- PANTHENOL (UNII: WV9CM0O67Z)
- ARGININE (UNII: 94ZLA3W45F)
- LACTIC ACID (UNII: 33X04XA5AT)
- TRICAPRIN (UNII: O1PB8EU98M)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- XANTHAN GUM (UNII: TTV12P4NEE)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
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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".