NDC 53208-460 Gongjinhyang Qi And Jin Eye
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 53208-460?
Which are Gongjinhyang Qi And Jin Eye UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972) (Active Moiety)
Which are Gongjinhyang Qi And Jin Eye 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SHEA BUTTER (UNII: K49155WL9Y)
- BETAINE (UNII: 3SCV180C9W)
- CAPRIC ACID (UNII: 4G9EDB6V73)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- 2-ETHYLHEXANOIC ACID (UNII: 01MU2J7VVZ)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PANTHENOL (UNII: WV9CM0O67Z)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- TROLAMINE (UNII: 9O3K93S3TK)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARBOMER 934 (UNII: Z135WT9208)
- PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
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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".