NDC 53208-500 Gongjinhyang Qi And Jin Eye
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53208 - Lg Household And Healthcare, Inc.
- 53208-500 - Gongjinhyang Qi And Jin Eye
Product Packages
NDC Code 53208-500-02
Package Description: 1 CONTAINER in 1 BOX / 20 mL in 1 CONTAINER (53208-500-01)
Product Details
What is NDC 53208-500?
What are the uses for Gongjinhyang Qi And Jin Eye?
Which are Gongjinhyang Qi And Jin Eye UNII Codes?
The UNII codes for the active ingredients in this product are:
- .GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I)
- .GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I) (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)
- PANTHENOL (UNII: WV9CM0O67Z)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ETHYLPARABEN (UNII: 14255EXE39)
- MACADAMIA OIL (UNII: 515610SU8C)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- AQUILARIA MALACCENSIS STEM (UNII: 3S41TU3DPS)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- 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".