NDC 83021-551 Anubismed
Spf 50 Broad Spectrum Protection Fluid Emulsion Cream Topical - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 83021 - Anubis Cosmetics Sl
- 83021-551 - Anubismed
Product Packages
NDC Code 83021-551-50
Package Description: 50 mL in 1 BOTTLE
Product Details
What is NDC 83021-551?
What are Anubismed Active Ingredients?
- .ALPHA.-TOCOPHEROL .006 g/50mL - A natural tocopherol and one of the most potent antioxidant tocopherols. It exhibits antioxidant activity by virtue of the phenolic hydrogen on the 2H-1-benzopyran-6-ol nucleus. It has four methyl groups on the 6-chromanol nucleus. The natural d form of alpha-tocopherol is more active than its synthetic dl-alpha-tocopherol racemic mixture.
- ANHYDROUS CITRIC ACID .00025 g/50mL - A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.
- ASCORBIC ACID .00025 g/50mL - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
- ASCORBYL PALMITATE .00125 g/50mL
- AVOBENZONE 1.8 g/50mL
- BEMOTRIZINOL 1.45 g/50mL
- BUTYLATED HYDROXYTOLUENE .0018 g/50mL - A di-tert-butyl PHENOL with antioxidant properties.
- BUTYLENE GLYCOL 2.5 g/50mL
- C20-22 ALCOHOLS .3375 g/50mL
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) .075 g/50mL
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE .025 g/50mL
- CHLORPHENESIN .1 g/50mL - A centrally acting muscle relaxant. Its mode of action is unknown. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1203)
- DIMETHICONE 1.25 g/50mL
- FRAGRANCE 13576 .3 g/50mL
- GLYCERIN .005 g/50mL
- LINOLEIC ACID .49725 g/50mL - A doubly unsaturated fatty acid, occurring widely in plant glycosides. It is an essential fatty acid in mammalian nutrition and is used in the biosynthesis of prostaglandins and cell membranes. (From Stedman, 26th ed)
- LINOLENIC ACID .00275 g/50mL
- OCTINOXATE 3.5982 g/50mL
- OCTISALATE 1.8 g/50mL
- OCTOCRYLENE 1.8 g/50mL
- PHENOXYETHANOL .35 g/50mL
- POLY(METHYL METHACRYLATE 2.1 g/50mL
- 450000 MW) .14225 g/50mL
- POLYETHYLENE GLYCOL 400 2.5 g/50mL
- PROPYLENE GLYCOL .575 g/50mL - A clear, colorless, viscous organic solvent and diluent used in pharmaceutical preparations.
- SILICON DIOXIDE .425 g/50mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
- TITANIUM DIOXIDE .22 g/50mL
- TROMETHAMINE 27.55 mL/50mL - An organic amine proton acceptor. It is used in the synthesis of surface-active agents and pharmaceuticals; as an emulsifying agent for cosmetic creams and lotions, mineral oil and paraffin wax emulsions, as a biological buffer, and used as an alkalizer. (From Merck, 11th ed; Martindale, The Extra Pharmacopoeia, 30th ed, p1424)
- WATER - 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:
- WATER (UNII: 059QF0KO0R)
- WATER (UNII: 059QF0KO0R) (Active Moiety)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) (Active Moiety)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
- LINOLENIC ACID (UNII: 0RBV727H71)
- LINOLENIC ACID (UNII: 0RBV727H71) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) (Active Moiety)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (Active Moiety)
- FRAGRANCE 13576 (UNII: 5EM498GW35)
- FRAGRANCE 13576 (UNII: 5EM498GW35) (Active Moiety)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L) (Active Moiety)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) (Active Moiety)
- POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
- POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T) (Active Moiety)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (Active Moiety)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- LINOLEIC ACID (UNII: 9KJL21T0QJ) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (Active Moiety)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- ASCORBYL PALMITATE (UNII: QN83US2B0N) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- BEMOTRIZINOL (UNII: PWZ1720CBH) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA) (Active Moiety)
- C20-22 ALCOHOLS (UNII: O4M0347C6A)
- C20-22 ALCOHOLS (UNII: O4M0347C6A) (Active Moiety)
- TROMETHAMINE (UNII: 023C2WHX2V)
- TROMETHAMINE (UNII: 023C2WHX2V) (Active Moiety)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CHLORPHENESIN (UNII: I670DAL4SZ) (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:
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- C20-22 ALKYL PHOSPHATE (UNII: L4VKP0Y7RP)
Which are the Pharmacologic Classes for Anubismed?
- Acidifying Activity - [MoA] (Mechanism of Action)
- Allergens - [CS]
- Anti-coagulant - [EPC] (Established Pharmacologic Class)
- Ascorbic Acid - [CS]
- Calcium Chelating Activity - [MoA] (Mechanism of Action)
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Decreased Coagulation Factor Activity - [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)
- Vitamin C - [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".