NDC 50184-6300 Hope In A Tinted Moisturizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50184 - Philosophy, Inc.
- 50184-6300 - Hope In A Tinted Moisturizer
Product Packages
NDC Code 50184-6300-1
Package Description: 50 mL in 1 TUBE
Product Details
What is NDC 50184-6300?
What are the uses for Hope In A Tinted Moisturizer?
Which are Hope In A Tinted Moisturizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Hope In A Tinted Moisturizer 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- DOCOSANOL (UNII: 9G1OE216XY)
- GLYCERIN (UNII: PDC6A3C0OX)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- MANGO (UNII: I629I3NR86)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- ENGLISH LAVENDER OIL (UNII: ZBP1YXW0H8)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALLANTOIN (UNII: 344S277G0Z)
- .BETA.-SITOSTEROL (UNII: S347WMO6M4)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- CARNOSINE (UNII: 8HO6PVN24W)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- POLYOXYL 40 CASTOR OIL (UNII: 4ERD2076EF)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- PPG-5-CETETH-20 (UNII: 4AAN25P8P4)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- DEXTRAN 1 (UNII: I8LHQ0D645)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- OCTYLTRIETHOXYSILANE (UNII: LDC331P08E)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
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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".