NDC 69579-102 P1p Chitosan V-mask
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69579 - Phytos Co., Ltd.
- 69579-102 - P1p Chitosan V-mask
Product Packages
NDC Code 69579-102-02
Package Description: 5 PATCH in 1 BOX / 25 mL in 1 PATCH (69579-102-01)
Product Details
What is NDC 69579-102?
Which are P1p Chitosan V-mask UNII Codes?
The UNII codes for the active ingredients in this product are:
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
- PANTHENOL (UNII: WV9CM0O67Z)
- PANTHENOL (UNII: WV9CM0O67Z) (Active Moiety)
Which are P1p Chitosan V-mask 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PEG-8 CAPRYLIC/CAPRIC GLYCERIDES (UNII: 00BT03FSO2)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TOTAROL (UNII: 67NH2854WW)
- TRANEXAMIC ACID (UNII: 6T84R30KC1)
- COLLAGEN ALPHA-1(III) (HUMAN) (UNII: 5D8UAE62VB)
- ETHYLHEXYL ETHYLHEXANOATE (UNII: 430RJA6715)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
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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".