NDC 67226-2330 Physical Facial Block Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 67226-2330?
What are the uses for Physical Facial Block Spf 30?
Which are Physical Facial Block Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Physical Facial Block 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:
- ALUMINUM OXIDE (UNII: LMI26O6933)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE (UNII: KBC00G95HI)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIPROPYLENE GLYCOL DIBENZOATE (UNII: 6OA5ZDY41O)
- ETHYLPARABEN (UNII: 14255EXE39)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PPG-15 STEARYL ETHER BENZOATE (UNII: 80D2J6361M)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- XANTHAN GUM (UNII: TTV12P4NEE)
- WATER (UNII: 059QF0KO0R)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SUGARCANE (UNII: 81H2R5AOH3)
- APPLE (UNII: B423VGH5S9)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- BIS-PEG/PPG-16/16 PEG/PPG-16/16 DIMETHICONE (UNII: 55A74AJ3KB)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)
- CITRUS BIOFLAVONOIDS (UNII: BD70459I50)
- EICOSYL POVIDONE (UNII: XQQ9MKE2BJ)
* Please review the disclaimer below.
[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".