NDC 43406-0709 Hemorrhoid Gel
Achillea Millefolium,Aesculus Hippocastanum,Hamamelis Virginiana,Ruscus Aculeatus,Aloe - View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 43406-0709?
What are the uses for Hemorrhoid Gel?
What are Hemorrhoid Gel Active Ingredients?
- ACHILLEA MILLEFOLIUM WHOLE 4 [hp_X]/g
- ALOE 6 [hp_X]/g - A plant genus of the family ASPHODELACEAE which is used medicinally. It contains anthraquinone glycosides such as aloin-emodin or aloe-emodin (EMODIN).
- CHELIDONIUM MAJUS WHOLE 30 [hp_C]/g
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 4 [hp_X]/g
- HORSE CHESTNUT 30 [hp_C]/g - A plant genus of the family HIPPOCASTANACEAE (or SAPINDACEAE by some) that contains antimicrobial protein 1 and escin. A. hippocastanum is used in folk medicine for treating chronic venous insufficiency.
- KRAMERIA LAPPACEA ROOT 30 [hp_C]/g
- NITRIC ACID 12 [hp_X]/g - Nitric acid (HNO3). A colorless liquid that is used in the manufacture of inorganic and organic nitrates and nitro compounds for fertilizers, dye intermediates, explosives, and many different organic chemicals. Continued exposure to vapor may cause chronic bronchitis; chemical pneumonitis may occur. (From Merck Index, 11th ed)
- PAEONIA OFFICINALIS ROOT 6 [hp_X]/g
- PHOSPHORUS 12 [hp_X]/g - 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.
- PODOPHYLLUM 12 [hp_X]/g - A genus of poisonous American herbs, family BERBERIDACEAE. The roots yield PODOPHYLLOTOXIN and other pharmacologically important agents. The plant was formerly used as a cholagogue and cathartic. It is different from the European mandrake, MANDRAGORA.
- PULSATILLA VULGARIS WHOLE 12 [hp_X]/g
- RUSCUS ACULEATUS WHOLE 4 [hp_X]/g
- STRYCHNOS IGNATII SEED 12 [hp_X]/g
- STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/g
- SULFUR 30 [hp_C]/g - 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.
Which are Hemorrhoid Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACHILLEA MILLEFOLIUM WHOLE (UNII: 2FXJ6SW4PK)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (Active Moiety)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
- RUSCUS ACULEATUS WHOLE (UNII: 5KEZ82GMGU)
- RUSCUS ACULEATUS WHOLE (UNII: 5KEZ82GMGU) (Active Moiety)
- ALOE (UNII: V5VD430YW9)
- ALOE (UNII: V5VD430YW9) (Active Moiety)
- PAEONIA OFFICINALIS ROOT (UNII: 8R564U2E1P)
- PAEONIA OFFICINALIS ROOT (UNII: 8R564U2E1P) (Active Moiety)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- PODOPHYLLUM (UNII: 2S713A4VP3)
- PODOPHYLLUM (UNII: 2S713A4VP3) (Active Moiety)
- PULSATILLA VULGARIS WHOLE (UNII: I76KB35JEV)
- ANEMONE PULSATILLA (UNII: I76KB35JEV) (Active Moiety)
- KRAMERIA LAPPACEA ROOT (UNII: P29ZH1A35Z)
- KRAMERIA LAPPACEA ROOT (UNII: P29ZH1A35Z) (Active Moiety)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ) (Active Moiety)
- CHELIDONIUM MAJUS WHOLE (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Hemorrhoid Gel 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:
- CARBOMER 980 (UNII: 4Q93RCW27E)
- ALCOHOL (UNII: 3K9958V90M)
- ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- GLYCERIN (UNII: PDC6A3C0OX)
Which are the Pharmacologic Classes for Hemorrhoid Gel?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
* 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.
[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 ("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".