NDC 67938-1094 Eight Hour Cream Sun Defense For Face Spf 50 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 67938-1094?
What are the uses for Eight Hour Cream Sun Defense For Face Spf 50 Sunscreen?
Which are Eight Hour Cream Sun Defense For Face Spf 50 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Eight Hour Cream Sun Defense For Face Spf 50 Sunscreen 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)
- ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- DOCOSANOL (UNII: 9G1OE216XY)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- SORBIC ACID (UNII: X045WJ989B)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
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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".