NDC 10477-1384 Zinc Oxide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 10477-1384?
What are the uses for Zinc Oxide?
Which are Zinc Oxide UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Zinc Oxide 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF POLYSACCHARIDES (UNII: W21O437517)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETETH-20 PHOSPHATE (UNII: 921FTA1500)
- OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- NERIUM OLEANDER LEAF (UNII: 7KV510R6H6)
- EGG SHELL MEMBRANE (UNII: N7QBR4212V)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
- SUPEROXIDE DISMUTASE (MN) SACCHAROMYCES CEREVISIAE (UNII: 0192074X0K)
- POLYGONUM AVICULARE WHOLE (UNII: M990N03611)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- NIACINAMIDE (UNII: 25X51I8RD4)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- OAT (UNII: Z6J799EAJK)
- MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)
- ROSEMARY (UNII: IJ67X351P9)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- PALMITOYLLYSYLVALYLDIAMINOBUTYROYLTHREONINE (UNII: 1615WE9073)
- PALMITOYL TRIPEPTIDE-5 (UNII: 2A3916MQHO)
- TETRADECYL AMINOBUTYROYLVALYLAMINOBUTYRIC UREA TRIFLUOROACETATE (UNII: 0UBP26S1LG)
- GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- XANTHAN GUM (UNII: TTV12P4NEE)
- DISODIUM ETHYLENEDIAMINEDIACETATE (UNII: EQL53S5L0F)
- PHENYLPROPANOL (UNII: 0F897O3O4M)
- DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- TROMETHAMINE (UNII: 023C2WHX2V)
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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".