NDC 61383-201 Photo Plasma
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 61383-201?
What are the uses for Photo Plasma?
Which are Photo Plasma UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Photo Plasma 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 HYDROXIDE (UNII: 5QB0T2IUN0)
- ASTAXANTHIN (UNII: 8XPW32PR7I)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- LEVOMENOL (UNII: 24WE03BX2T)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
- POLYGLYCERYL-3 LAURATE (UNII: Y9ZSR39D0E)
- POLYSILICONE-15 (UNII: F8DRP5BB29)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- .ALPHA.-LIPOIC ACID (UNII: 73Y7P0K73Y)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
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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".