NDC 53208-459 Bamboo Salt Eunganggo Jook Yeom Toothpaste
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53208 - Lg Household And Healthcare, Inc.
- 53208-459 - Bamboo Salt Eunganggo Jook Yeom Toothpaste
Product Packages
NDC Code 53208-459-02
Package Description: 1 TUBE in 1 CARTON / 170 g in 1 TUBE (53208-459-01)
Product Details
What is NDC 53208-459?
Which are Bamboo Salt Eunganggo Jook Yeom Toothpaste UNII Codes?
The UNII codes for the active ingredients in this product are:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- AMINOCAPROIC ACID (UNII: U6F3787206)
- AMINOCAPROIC ACID (UNII: U6F3787206) (Active Moiety)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) (Active Moiety)
- URSODIOL (UNII: 724L30Y2QR)
- URSODIOL (UNII: 724L30Y2QR) (Active Moiety)
- CURCUMA XANTHORRHIZA OIL (UNII: F8VF0V2G7H)
- CURCUMA XANTHORRHIZA OIL (UNII: F8VF0V2G7H) (Active Moiety)
- SEA SALT (UNII: 87GE52P74G)
- SEA SALT (UNII: 87GE52P74G) (Active Moiety)
Which are Bamboo Salt Eunganggo Jook Yeom Toothpaste 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:
- SORBITOL (UNII: 506T60A25R)
- POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM BISULFITE (UNII: TZX5469Z6I)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WATER (UNII: 059QF0KO0R)
- PEPPERMINT (UNII: V95R5KMY2B)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
* Please review the disclaimer below.
[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".