NDC 79814-008 Mastikis Mastic 24k Whitening
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79814 - Mastic Korea.co.ltd
- 79814-008 - Mastikis Mastic 24k Whitening
Product Packages
NDC Code 79814-008-02
Package Description: 1 TUBE in 1 CARTON / 110 g in 1 TUBE (79814-008-01)
Product Details
What is NDC 79814-008?
What are the uses for Mastikis Mastic 24k Whitening?
Which are Mastikis Mastic 24k Whitening UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V) (Active Moiety)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are Mastikis Mastic 24k Whitening 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)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- XYLITOL (UNII: VCQ006KQ1E)
- STEVIOSIDE (UNII: 0YON5MXJ9P)
- CITRUS PARADISI SEED (UNII: 12F08874Y7)
- SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
- SPEARMINT OIL (UNII: C3M81465G5)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- LICORICE (UNII: 61ZBX54883)
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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".