NDC 83021-750 Anubismed
Ha Hyaluronic Cream Topical - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 83021 - Anubis Cosmetics Sl
- 83021-750 - Anubismed
Product Packages
NDC Code 83021-750-50
Package Description: 50 mL in 1 JAR
Product Details
What is NDC 83021-750?
What are Anubismed Active Ingredients?
- 1,2-HEXANEDIOL .198 g/50mL
- ALLANTOIN .05 g/50mL - A urea hydantoin that is found in URINE and PLANTS and is used in dermatological preparations.
- ALOE VERA LEAF 2.5 g/50mL
- BUTYLATED HYDROXYTOLUENE .0535 g/50mL - A di-tert-butyl PHENOL with antioxidant properties.
- C12-20 ACID PEG-8 ESTER 2.25 g/50mL
- CAPRYLYL GLYCOL .198 g/50mL
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE .25 g/50mL
- CETEARYL ETHYLHEXANOATE 1.75 g/50mL
- CETYL ALCOHOL .0038 g/50mL
- DECYL OLEATE 1.9996 g/50mL
- DIMETHICONE .25 g/50mL
- FRAGRANCE 13576 .225 g/50mL
- GLYCERIN .4975 g/50mL
- GLYCERYL MONOSTEARATE .875 g/50mL
- GLYCERYL STEARATE SE 1.5 g/50mL
- IMIDUREA .15 g/50mL
- MEDIUM-CHAIN TRIGLYCERIDES 1.5 g/50mL
- OCTINOXATE 3.4965 g/50mL
- OXYBENZONE 2 g/50mL
- PROPYLENE GLYCOL 1.996 g/50mL - A clear, colorless, viscous organic solvent and diluent used in pharmaceutical preparations.
- TOCOPHEROL .0004 g/50mL
- TROLAMINE .3 g/50mL
- TROPOLONE .004 g/50mL - A seven-membered aromatic ring compound. It is structurally related to a number of naturally occurring antifungal compounds (ANTIFUNGAL AGENTS).
- WATER 27.4065 mL/50mL - A clear, odorless, tasteless liquid that is essential for most animal and plant life and is an excellent solvent for many substances. The chemical formula is hydrogen oxide (H2O). (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
Which are Anubismed UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALOE VERA LEAF (UNII: ZY81Z83H0X) (Active Moiety)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) (Active Moiety)
- TROLAMINE (UNII: 9O3K93S3TK)
- TROLAMINE (UNII: 9O3K93S3TK) (Active Moiety)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) (Active Moiety)
- FRAGRANCE 13576 (UNII: 5EM498GW35)
- FRAGRANCE 13576 (UNII: 5EM498GW35) (Active Moiety)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (Active Moiety)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETYL ALCOHOL (UNII: 936JST6JCN) (Active Moiety)
- TROPOLONE (UNII: 7L6DL16P1T)
- TROPOLONE (UNII: 7L6DL16P1T) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G) (Active Moiety)
- IMIDUREA (UNII: M629807ATL)
- IMIDUREA (UNII: M629807ATL) (Active Moiety)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) (Active Moiety)
- CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)
- CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25) (Active Moiety)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) (Active Moiety)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TOCOPHEROL (UNII: R0ZB2556P8) (Active Moiety)
- WATER (UNII: 059QF0KO0R)
- WATER (UNII: 059QF0KO0R) (Active Moiety)
- C12-20 ACID PEG-8 ESTER (UNII: 9M7A3K4339)
- C12-20 ACID PEG-8 ESTER (UNII: 9M7A3K4339) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I) (Active Moiety)
- DECYL OLEATE (UNII: ZGR06DO97T)
- DECYL OLEATE (UNII: ZGR06DO97T) (Active Moiety)
Which are Anubismed 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:
- SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)
- CETYL PHOSPHATE (UNII: VT07D6X67O)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
Which are the Pharmacologic Classes for Anubismed?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Glycerol - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
- Skin Barrier Activity - [PE] (Physiologic Effect)
- Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[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.
[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
[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".