NDC 53208-531 Isaknox X202 Whitening Secret Essence
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53208 - Lg Household And Healthcare, Inc.
- 53208-531 - Isaknox X202 Whitening Secret Essence
Product Packages
NDC Code 53208-531-02
Package Description: 1 CONTAINER in 1 BOX / 50 mL in 1 CONTAINER (53208-531-01)
Product Details
What is NDC 53208-531?
What are the uses for Isaknox X202 Whitening Secret Essence?
Which are Isaknox X202 Whitening Secret Essence UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIOSMETIN (UNII: TWZ37241OT)
- DIOSMETIN (UNII: TWZ37241OT) (Active Moiety)
Which are Isaknox X202 Whitening Secret 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)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
- GLYCERIN (UNII: PDC6A3C0OX)
- DOCOSANOL (UNII: 9G1OE216XY)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ALCOHOL (UNII: 3K9958V90M)
- PONCIRUS TRIFOLIATA FRUIT (UNII: 44445L49J2)
- ETHYLPARABEN (UNII: 14255EXE39)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- NIACINAMIDE (UNII: 25X51I8RD4)
- PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
- CANNA INDICA ROOT (UNII: BZK836AQFQ)
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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".