NDC 53208-414 Isa Knox White Symphony Ampule Essence
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53208 - Lg Household And Healthcare, Inc.
- 53208-414 - Isa Knox White Symphony Ampule Essence
Product Packages
NDC Code 53208-414-02
Package Description: 1 CONTAINER in 1 BOX / 50 mL in 1 CONTAINER (53208-414-01)
Product Details
What is NDC 53208-414?
Which are Isa Knox White Symphony Ampule Essence UNII Codes?
The UNII codes for the active ingredients in this product are:
- ATRACTYLODES JAPONICA ROOT (UNII: 58N5X5H9XU)
- ATRACTYLODES JAPONICA ROOT (UNII: 58N5X5H9XU) (Active Moiety)
Which are Isa Knox White Symphony Ampule Essence 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)
- ALCOHOL (UNII: 3K9958V90M)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- 2-ETHYLHEXANOIC ACID (UNII: 01MU2J7VVZ)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAPRIC ACID (UNII: 4G9EDB6V73)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PANTHENOL (UNII: WV9CM0O67Z)
- BETAINE (UNII: 3SCV180C9W)
- TROLAMINE (UNII: 9O3K93S3TK)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- EDETATE TRISODIUM (UNII: 420IP921MB)
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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".