NDC 83021-546 Anubis Barcelona
Dmae Concentrate Topical - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 83021-546?
What are Anubis Barcelona Active Ingredients?
- ASCORBYL GLUCOSIDE .15 g/30mL
- BENZOIC ACID .036 g/30mL - A fungistatic compound that is widely used as a food preservative. It is conjugated to GLYCINE in the liver and excreted as hippuric acid.
- DEHYDROACETIC ACID .021 g/30mL
- DICAPRYLYL ETHER .9 g/30mL
- FRAGRANCE 13576 .027 g/30mL
- GLYCERIN .555 g/30mL
- HYDROLYZED BOVINE ELASTIN (BASE .0012 g/30mL
- 1000 MW) .0006 g/30mL
- HYDROXYCITRONELLAL .405 g/30mL
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) .45 g/30mL
- LECITHIN, SOYBEAN .0009 g/30mL
- LIMONENE, (+)- .243 g/30mL
- PHENOXYETHANOL .024 g/30mL
- POLYSORBATE 60 1.08 g/30mL
- PROPANEDIOL .024 g/30mL
- SORBITAN ISOSTEARATE .0003 g/30mL
- TOCOPHEROL 25.5564 mL/30mL
- WATER .09 g/30mL - 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)
- XANTHAN GUM
Which are Anubis Barcelona UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T) (Active Moiety)
- XANTHAN GUM (UNII: TTV12P4NEE)
- XANTHAN GUM (UNII: TTV12P4NEE) (Active Moiety)
- FRAGRANCE 13576 (UNII: 5EM498GW35)
- FRAGRANCE 13576 (UNII: 5EM498GW35) (Active Moiety)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) (Active Moiety)
- HYDROLYZED BOVINE ELASTIN (BASE; 1000 MW) (UNII: ZR28QKN0WT)
- HYDROLYZED BOVINE ELASTIN (BASE; 1000 MW) (UNII: ZR28QKN0WT) (Active Moiety)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- LIMONENE, (+)- (UNII: GFD7C86Q1W) (Active Moiety)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TOCOPHEROL (UNII: R0ZB2556P8) (Active Moiety)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR) (Active Moiety)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62) (Active Moiety)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) (Active Moiety)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R) (Active Moiety)
- PROPANEDIOL (UNII: 5965N8W85T)
- PROPANEDIOL (UNII: 5965N8W85T) (Active Moiety)
- DICAPRYLYL ETHER (UNII: 77JZM5516Z)
- DICAPRYLYL ETHER (UNII: 77JZM5516Z) (Active Moiety)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- BENZOIC ACID (UNII: 8SKN0B0MIM) (Active Moiety)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW) (Active Moiety)
- WATER (UNII: 059QF0KO0R)
- WATER (UNII: 059QF0KO0R) (Active Moiety)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- POLYSORBATE 60 (UNII: CAL22UVI4M) (Active Moiety)
Which are Anubis Barcelona 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:
- DEANOL (UNII: 2N6K9DRA24)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PHYTATE SODIUM (UNII: 88496G1ERL)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
Which are the Pharmacologic Classes for Anubis Barcelona?
- Allergens - [CS]
- Allergens - [CS]
- Ammonium Ion Binding Activity - [MoA] (Mechanism of Action)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Glycerol - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Nitrogen Binding Agent - [EPC] (Established Pharmacologic Class)
- Non-Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
- 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".