NDC 82224-001 Ribeskin Epiderm Plus Mask
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 82224-001?
What are the uses for Ribeskin Epiderm Plus Mask?
Which are Ribeskin Epiderm Plus Mask UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
- CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)
- CENTELLA ASIATICA (UNII: 7M867G6T1U) (Active Moiety)
- NEPIDERMIN (UNII: TZK30RF92W)
- HUMAN EPIDERMAL GROWTH FACTOR (UNII: TZK30RF92W) (Active Moiety)
- GIANT AFRICAN SNAIL (UNII: 5A1SK0DCIZ)
- GIANT AFRICAN SNAIL (UNII: 5A1SK0DCIZ) (Active Moiety)
Which are Ribeskin Epiderm Plus 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- C12-14 PARETH-12 (UNII: M0LJS773XW)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- TROMETHAMINE (UNII: 023C2WHX2V)
- PROPANEDIOL (UNII: 5965N8W85T)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PANTHENOL (UNII: WV9CM0O67Z)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- STAR ANISE FRUIT (UNII: CK15HA8438)
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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".