NDC 53208-503 The History Of Whoo Jin Hae Yoon Sun
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53208 - Lg Household And Healthcare, Inc.
- 53208-503 - The History Of Whoo Jin Hae Yoon Sun
Product Packages
NDC Code 53208-503-02
Package Description: 1 CONTAINER in 1 BOX / 60 mL in 1 CONTAINER (53208-503-01)
Product Details
What is NDC 53208-503?
Which are The History Of Whoo Jin Hae Yoon Sun UNII Codes?
The UNII codes for the active ingredients in this product are:
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- BEMOTRIZINOL (UNII: PWZ1720CBH) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- AMILOXATE (UNII: 376KTP06K8)
- AMILOXATE (UNII: 376KTP06K8) (Active Moiety)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20) (Active Moiety)
Which are The History Of Whoo Jin Hae Yoon Sun 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)
- TROMETHAMINE (UNII: 023C2WHX2V)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL PHOSPHATE (UNII: VT07D6X67O)
- FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS)
- PANTHENOL (UNII: WV9CM0O67Z)
- ALCOHOL (UNII: 3K9958V90M)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ETHYLPARABEN (UNII: 14255EXE39)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- FRUIT (UNII: C2AIY4ERZC)
- TROLAMINE (UNII: 9O3K93S3TK)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- AQUILARIA MALACCENSIS STEM (UNII: 3S41TU3DPS)
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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".