NDC 59779-624 Kids Disappearing Color Spf50 Broad Spectrum Suncreen Pink Strawberry Scented
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 59779-624?
What are the uses for Kids Disappearing Color Spf50 Broad Spectrum Suncreen Pink Strawberry Scented?
Which are Kids Disappearing Color Spf50 Broad Spectrum Suncreen Pink Strawberry Scented 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 Kids Disappearing Color Spf50 Broad Spectrum Suncreen Pink Strawberry Scented 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)
- PROPANE (UNII: T75W9911L6)
- BUTANE (UNII: 6LV4FOR43R)
- ISOBUTANE (UNII: BXR49TP611)
- ALCOHOL (UNII: 3K9958V90M)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STYRENE (UNII: 44LJ2U959V)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- TRICONTANYL POVIDONE (4 TRICONTANYL BRANCHES/REPEAT) (UNII: N0SS3Q238D)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- ALLANTOIN (UNII: 344S277G0Z)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- POLYGLYCERYL-10 STEARATE (UNII: 90TF85HH91)
- DOCOSANOL (UNII: 9G1OE216XY)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ASTAXANTHIN (UNII: 8XPW32PR7I)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PANTHENOL (UNII: WV9CM0O67Z)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
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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".