NDC 61500-5547 Topricin
Aesculus Hippocastanum,Arnica Montana,Belladonna,Calendula Officinalis,Crotalus - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 61500-5547?
What are the uses for Topricin?
What are Topricin Active Ingredients?
- AESCULUS HIPPOCASTANUM FLOWER 6 [hp_X]/227g
- ARNICA MONTANA 6 [hp_X]/227g
- ATROPA BELLADONNA 6 [hp_X]/227g - A plant species of the genus ATROPA, family SOLANACEAE that contains ATROPINE; SCOPOLAMINE; BELLADONNA ALKALOIDS and other SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for SOLANUM.
- CALENDULA OFFICINALIS FLOWERING TOP 4 [hp_X]/227g
- CROTALUS HORRIDUS HORRIDUS VENOM 8 [hp_X]/227g
- ECHINACEA ANGUSTIFOLIA 4 [hp_X]/227g - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- GRAPHITE 6 [hp_X]/227g - An allotropic form of carbon that is used in pencils, as a lubricant, and in matches and explosives. It is obtained by mining and its dust can cause lung irritation.
- HELODERMA HORRIDUM VENOM 8 [hp_X]/227g
- LACHESIS MUTA VENOM 8 [hp_X]/227g
- NAJA NAJA VENOM 8 [hp_X]/227g
- PHOSPHORUS 9 [hp_X]/227g - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
- RUTA GRAVEOLENS FLOWERING TOP 6 [hp_X]/227g
- SULFUR 8 [hp_X]/227g - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
- TOXICODENDRON PUBESCENS LEAF 8 [hp_X]/227g
Which are Topricin UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- CROTALUS HORRIDUS HORRIDUS VENOM (UNII: YHA2XLJ956)
- CROTALUS HORRIDUS HORRIDUS VENOM (UNII: YHA2XLJ956) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- HELODERMA HORRIDUM VENOM (UNII: O9M1UQ4YIO)
- HELODERMA HORRIDUM VENOM (UNII: O9M1UQ4YIO) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- NAJA NAJA VENOM (UNII: ZZ4AG7L7VM)
- NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
- AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M)
- AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Topricin 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:
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEG-100 STEARATE (UNII: YD01N1999R)
- WATER (UNII: 059QF0KO0R)
- STEARETH-21 (UNII: 53J3F32P58)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HYDROGENATED PALM KERNEL OIL (UNII: FM8D1RE2VP)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
* 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.
[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".