NDC 65903-171 Uv Defense Fluid
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 65903-171?
What are the uses for Uv Defense Fluid?
Which are Uv Defense Fluid UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Uv Defense Fluid 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)
- WATER (UNII: 059QF0KO0R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- FERULIC ACID (UNII: AVM951ZWST)
- GLYCERIN (UNII: PDC6A3C0OX)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- ISODECYL ISONONANOATE (UNII: 4X46Q4U00Z)
- LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PHYLLANTHUS EMBLICA FRUIT (UNII: YLX4CW2576)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ROSEMARY (UNII: IJ67X351P9)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SORBIC ACID (UNII: X045WJ989B)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TETRAHYDRODIFERULOYLMETHANE (UNII: 00U0645U03)
- TOCOPHEROL (UNII: R0ZB2556P8)
- UNDARIA PINNATIFIDA (UNII: ICV1OK7M1S)
- BENZYL BENZOATE (UNII: N863NB338G)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- LIMONENE, (-)- (UNII: 47MAJ1Y2NE)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
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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".