NDC 11822-3430 Daylogic Tinted Daily Moisturizer Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11822 - Rite Aid Corporation
- 11822-3430 - Daylogic Tinted Daily Moisturizer Spf 30
Product Packages
NDC Code 11822-3430-1
Package Description: 50 mL in 1 TUBE
Product Details
What is NDC 11822-3430?
What are the uses for Daylogic Tinted Daily Moisturizer Spf 30?
Which are Daylogic Tinted Daily Moisturizer Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- ENSULIZOLE (UNII: 9YQ9DI1W42) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Daylogic Tinted Daily Moisturizer 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:
- WATER (UNII: 059QF0KO0R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- TRIMETHYLOLPROPANE TRIETHYLHEXANOATE (UNII: B952ZGW1IL)
- PEG-100 STEARATE (UNII: YD01N1999R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- TROLAMINE (UNII: 9O3K93S3TK)
- DOCOSANOL (UNII: 9G1OE216XY)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
- LEVOMENOL (UNII: 24WE03BX2T)
- DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
- CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CODIUM TOMENTOSUM (UNII: B8B45BRU87)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SODIUM ACRYLATE (UNII: 7C98FKB43H)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".