NDC 76214-002 Goldkiwi
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 76214-002?
What are the uses for Goldkiwi?
Which are Goldkiwi UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Goldkiwi 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)
- ACTINIDIA CHINENSIS SEED (UNII: 53V4NSR15J)
- TRISILOXANE (UNII: 9G1ZW13R0G)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERIN (UNII: PDC6A3C0OX)
- NIACINAMIDE (UNII: 25X51I8RD4)
- BETAINE (UNII: 3SCV180C9W)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- MACADAMIA OIL (UNII: 515610SU8C)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- C14-22 ALCOHOLS (UNII: B1K89384RJ)
- MAACKIA FLORIBUNDA STEM (UNII: 84UXW52K8Y)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)
- PRUNUS MUME FRUIT (UNII: 639190I8CU)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- NYMPHAEA ALBA FLOWER (UNII: 40KQ7Q535O)
- SODIUM PALMITOYL PROLINE (UNII: 64L053FRFO)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- XANTHAN GUM (UNII: TTV12P4NEE)
- DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
- PANTHENOL (UNII: WV9CM0O67Z)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- WHEAT GERM (UNII: YR3G369F5A)
What is the NDC to RxNorm Crosswalk for Goldkiwi?
- RxCUI: 1116931 - dimethicone 6.7 % Topical Cream
- RxCUI: 1116931 - dimethicone 67 MG/ML Topical Cream
* 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".