NDC 70686-102 Pixi Sun Serum Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 70686-102?
What are the uses for Pixi Sun Serum Spf 30?
Which are Pixi Sun Serum Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Pixi Sun Serum 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- STARCH, CORN (UNII: O8232NY3SJ)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- SQUALANE (UNII: GW89575KF9)
- GLYCERIN (UNII: PDC6A3C0OX)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SOYBEAN OIL (UNII: 241ATL177A)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
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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".