NDC 70889-300 Seolheun Ginseng Nature Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70889 - Oneskin Cosmetics Co., Ltd.
- 70889-300 - Seolheun Ginseng Nature Cream
Product Characteristics
Product Packages
NDC Code 70889-300-01
Package Description: 1 CONTAINER in 1 BOX / 50 mL in 1 CONTAINER
Product Details
What is NDC 70889-300?
What are the uses for Seolheun Ginseng Nature Cream?
Which are Seolheun Ginseng Nature Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
Which are Seolheun Ginseng Nature Cream 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ROBINIA PSEUDOACACIA FLOWER (UNII: U03189OIJ4)
- GLYCERIN (UNII: PDC6A3C0OX)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- BETAINE (UNII: 3SCV180C9W)
- ARGININE (UNII: 94ZLA3W45F)
- ALLANTOIN (UNII: 344S277G0Z)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GINGER (UNII: C5529G5JPQ)
- SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C)
- COPTIS JAPONICA WHOLE (UNII: 8BO3NHJ535)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- EDETIC ACID (UNII: 9G34HU7RV0)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HYACINTHUS ORIENTALIS WHOLE (UNII: 33J37WGZ7H)
- JASMINUM SAMBAC FLOWER (UNII: 2S686I937F)
- NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)
- SAMBUCUS NIGRA FLOWER (UNII: 07V4DX094T)
- PRUNUS MUME FLOWER (UNII: 2N8872050J)
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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".