NDC 71447-053 Nelly Devuyst Bio Medical Bioacne Anti-redness 50g
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What is NDC 71447-053?
What are the uses for Nelly Devuyst Bio Medical Bioacne Anti-redness 50g?
Which are Nelly Devuyst Bio Medical Bioacne Anti-redness 50g UNII Codes?
The UNII codes for the active ingredients in this product are:
- OATMEAL (UNII: 8PI54V663Y)
- OATMEAL (UNII: 8PI54V663Y) (Active Moiety)
Which are Nelly Devuyst Bio Medical Bioacne Anti-redness 50g 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:
- LEVOMENOL (UNII: 24WE03BX2T)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- CAPER BERRY (UNII: 7G4C45EE8C)
- PROPANEDIOL (UNII: 5965N8W85T)
- NELUMBO NUCIFERA ROOT OIL (UNII: 382005USDH)
- GLYCERIN (UNII: PDC6A3C0OX)
- TOCOPHEROL (UNII: R0ZB2556P8)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- XANTHAN GUM (UNII: TTV12P4NEE)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SORBIC ACID (UNII: X045WJ989B)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- .ALPHA.-GLUCAN OLIGOSACCHARIDE (UNII: S95658MI3W)
- WATER (UNII: 059QF0KO0R)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- FRUCTOSE (UNII: 6YSS42VSEV)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- OCTYLDODECYL MYRISTATE (UNII: S013N99GR8)
- INULIN (UNII: JOS53KRJ01)
What is the NDC to RxNorm Crosswalk for Nelly Devuyst Bio Medical Bioacne Anti-redness 50g?
- RxCUI: 2590666 - colloidal oatmeal 1.3 % Topical Gel
- RxCUI: 2590666 - colloidal oatmeal 0.013 MG/MG Topical Gel
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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".