NDC 81459-302 Repuera Dermatozyme 5% Ultra Moisture Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Get all the details for National Drug Code (NDC) 81459-302 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.
Code Structure Chart
Product Details
What is NDC 81459-302?
What are the uses for Repuera Dermatozyme 5% Ultra Moisture Cream?
Which are Repuera Dermatozyme 5% Ultra Moisture Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are Repuera Dermatozyme 5% Ultra Moisture 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:
- DOCOSANOL (UNII: 9G1OE216XY)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- RICE GERM (UNII: 7N2B70SFEZ)
- PINUS DENSIFLORA LEAF (UNII: Q1Q9P50WIY)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- CHAMOMILE (UNII: FGL3685T2X)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SAGE OIL (UNII: U27K0H1H2O)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HYDROGENATED POLY(C6-14 OLEFIN; 2 CST) (UNII: P0TX083987)
- HYDROGENATED POLYDECENE (1500 CST) (UNII: 4YI0729529)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)
- ICODEXTRIN (UNII: 2NX48Z0A9G)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- CERAMIDE NP (UNII: 4370DF050B)
- POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE (UNII: W19EIO0DBE)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- JUNIPERUS DEPPEANA WOOD OIL (UNII: 4739QA5686)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
- WATER (UNII: 059QF0KO0R)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ROSEMARY (UNII: IJ67X351P9)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- TROMETHAMINE (UNII: 023C2WHX2V)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- PREZATIDE COPPER (UNII: 6BJQ43T1I9)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- POLYGONUM CUSPIDATUM ROOT (UNII: 7TRV45YZF7)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- SHEA BUTTER (UNII: K49155WL9Y)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".