NDC 81459-303 Repuera Dermatozyme 5% Hydro Essential Ampule
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 81459-303?
What are the uses for Repuera Dermatozyme 5% Hydro Essential Ampule?
Which are Repuera Dermatozyme 5% Hydro Essential Ampule UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Repuera Dermatozyme 5% Hydro Essential Ampule 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:
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW) (UNII: 1394NXB9L6)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- DIPHENYL DIMETHICONE (100 CST) (UNII: AG1ANB6B8O)
- CHAMOMILE (UNII: FGL3685T2X)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549)
- POLYGONUM CUSPIDATUM ROOT (UNII: 7TRV45YZF7)
- DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3)
- JUNIPERUS DEPPEANA WOOD OIL (UNII: 4739QA5686)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- WATER (UNII: 059QF0KO0R)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- PREZATIDE COPPER (UNII: 6BJQ43T1I9)
- VALYLTRYPTOPHAN (UNII: 3G64B4AFQN)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- PINUS DENSIFLORA LEAF (UNII: Q1Q9P50WIY)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- SAGE OIL (UNII: U27K0H1H2O)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- PHYTOSTERYL/OCTYLDODECYL LAUROYL GLUTAMATE (UNII: 65954KGO9Q)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- XANTHAN GUM (UNII: TTV12P4NEE)
- GERANIOL (UNII: L837108USY)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- CERAMIDE NP (UNII: 4370DF050B)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PREZATIDE (UNII: 39TG2H631E)
- PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG)
- RICE GERM (UNII: 7N2B70SFEZ)
- ROSEMARY (UNII: IJ67X351P9)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- GELLAN GUM (LOW ACYL) (UNII: 7593U09I4D)
* Please review the disclaimer below.
[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".