NDC 76214-010 Gold Caviar Serum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 76214-010?
What are the uses for Gold Caviar Serum?
Which are Gold Caviar Serum UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Gold Caviar Serum 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:
- CAVIAR (UNII: 020K6HLU0O)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERETH-26 (UNII: NNE56F2N14)
- BETAINE (UNII: 3SCV180C9W)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- TRISILOXANE (UNII: 9G1ZW13R0G)
- NIACINAMIDE (UNII: 25X51I8RD4)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- JOJOBA OIL (UNII: 724GKU717M)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PROLINE (UNII: 9DLQ4CIU6V)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- SOYBEAN (UNII: L7HT8F1ZOD)
- PERSEA AMERICANA VAR. AMERICANA LEAF (UNII: 8490RQ2BET)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE)
- ADENOSINE (UNII: K72T3FS567)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- GOLD (UNII: 79Y1949PYO)
- CERAMIDE 3 (UNII: 4370DF050B)
- CARAMEL (UNII: T9D99G2B1R)
* 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".