NDC 53208-501 O Hui White Extreme Cellight
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53208 - Lg Household And Healthcare, Inc.
- 53208-501 - O Hui White Extreme Cellight
Product Packages
NDC Code 53208-501-02
Package Description: 1 CONTAINER in 1 BOX / 150 mL in 1 CONTAINER (53208-501-01)
Product Details
What is NDC 53208-501?
What are the uses for O Hui White Extreme Cellight?
Which are O Hui White Extreme Cellight UNII Codes?
The UNII codes for the active ingredients in this product are:
- PROTOCATECHUALDEHYDE (UNII: 4PVP2HCH4T)
- PROTOCATECHUALDEHYDE (UNII: 4PVP2HCH4T) (Active Moiety)
Which are O Hui White Extreme Cellight 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- ALCOHOL (UNII: 3K9958V90M)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ETHYLPARABEN (UNII: 14255EXE39)
- FRUIT (UNII: C2AIY4ERZC)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BETAINE (UNII: 3SCV180C9W)
- PANTHENOL (UNII: WV9CM0O67Z)
- COPPER (UNII: 789U1901C5)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
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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".