NDC 55628-8477 Spf Rx - Anti-aging Sunscreen Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55628 - Cal Pharma Llc
- 55628-8477 - Spf Rx - Anti-aging Sunscreen Spf 30
Product Packages
NDC Code 55628-8477-4
Package Description: 120 g in 1 TUBE
Product Details
What is NDC 55628-8477?
What are the uses for Spf Rx - Anti-aging Sunscreen Spf 30?
Which are Spf Rx - Anti-aging Sunscreen Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Spf Rx - Anti-aging Sunscreen Spf 30 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:
- (C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8)
- ALEURITES MOLUCCANA SEED (UNII: J87WJ3E7VW)
- ALLANTOIN (UNII: 344S277G0Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- C12-13 ALCOHOLS (UNII: T7ZJT3I9X2)
- DODECYL BENZOATE (UNII: N4F51K239A)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL PHOSPHATE (UNII: VT07D6X67O)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- MACADAMIA OIL (UNII: 515610SU8C)
- MAGNESIUM SILICATE (UNII: 9B9691B2N9)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- SQUALANE (UNII: GW89575KF9)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- TOCOPHEROL (UNII: R0ZB2556P8)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
* 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".