NDC 72630-020 Dr.plinus Fillincell Multi
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72630 - S Skin Co., Ltd.
- 72630-020 - Dr.plinus Fillincell Multi
Product Packages
NDC Code 72630-020-02
Package Description: 2 PATCH in 1 CONTAINER / .3 g in 1 PATCH (72630-020-01)
Product Details
What is NDC 72630-020?
What are the uses for Dr.plinus Fillincell Multi?
Which are Dr.plinus Fillincell Multi UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- HYALURONIC ACID (UNII: S270N0TRQY) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
Which are Dr.plinus Fillincell Multi 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)
- PROPANEDIOL (UNII: 5965N8W85T)
- GLYCERIN (UNII: PDC6A3C0OX)
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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".