NDC 69579-105 P1p Magic Whitening Antiaging
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69579 - Phytos Co., Ltd.
- 69579-105 - P1p Magic Whitening Antiaging
Product Packages
NDC Code 69579-105-02
Package Description: 1 AMPULE in 1 CARTON / 30 mL in 1 AMPULE (69579-105-01)
Product Details
What is NDC 69579-105?
Which are P1p Magic Whitening Antiaging UNII Codes?
The UNII codes for the active ingredients in this product are:
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- PANTHENOL (UNII: WV9CM0O67Z)
- PANTHENOL (UNII: WV9CM0O67Z) (Active Moiety)
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
Which are P1p Magic Whitening Antiaging 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)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- TRANEXAMIC ACID (UNII: 6T84R30KC1)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- SALIX ALBA BARK (UNII: 205MXS71H7)
- MORUS ALBA BARK (UNII: 7O71A48NDP)
- PAEONIA SUFFRUTICOSA ROOT (UNII: 7M7E9A2C8J)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- GLYCERIN (UNII: PDC6A3C0OX)
- 3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- 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".