NDC 76049-715 Stila Hydrating Primer Oil-free Spf 30 (all Shades)
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 76049-715?
What are the uses for Stila Hydrating Primer Oil-free Spf 30 (all Shades)?
Which are Stila Hydrating Primer Oil-free Spf 30 (all Shades) UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Stila Hydrating Primer Oil-free Spf 30 (all Shades) 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)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SHEA BUTTER (UNII: K49155WL9Y)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- COCO GLUCOSIDE (UNII: ICS790225B)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- SQUALANE (UNII: GW89575KF9)
- EUROPEAN HAZELNUT OIL (UNII: 8RQ2839AVG)
- JOJOBA OIL (UNII: 724GKU717M)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DOCOSANOL (UNII: 9G1OE216XY)
- PALMITIC ACID (UNII: 2V16EO95H1)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- LAURYL ALCOHOL (UNII: 178A96NLP2)
- MYRISTYL ALCOHOL (UNII: V42034O9PU)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- LEVOMENOL (UNII: 24WE03BX2T)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- LACTIC ACID (UNII: 33X04XA5AT)
- SERINE (UNII: 452VLY9402)
- UREA (UNII: 8W8T17847W)
- SORBITOL (UNII: 506T60A25R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ALLANTOIN (UNII: 344S277G0Z)
- CUCUMBER SEED OIL (UNII: AKP926H71P)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- O-CYMEN-5-OL (UNII: H41B6Q1I9L)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
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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".