NDC 66096-168 Acne Relief
Antimonium Crud,Arsenicum Brom,Bovista,Eugenia Jamb,Fluoricum Acidum,Hepar Sulph Calc,Kali - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 66096-168?
What are Acne Relief Active Ingredients?
- ANTIMONY TRISULFIDE 6 [hp_X]/59mL
- ARSENIC TRIBROMIDE 30 [hp_C]/59mL
- CALCIUM SULFIDE 30 [hp_C]/59mL
- HYDROFLUORIC ACID 30 [hp_C]/59mL - Hydrofluoric acid. A solution of hydrogen fluoride in water. It is a colorless fuming liquid which can cause painful burns.
- LYCOPERDON UTRIFORME FRUITING BODY 30 [hp_C]/59mL
- NICKEL SULFATE HEXAHYDRATE 4 [hp_X]/59mL
- PHOSPHORIC ACID 30 [hp_C]/59mL
- POTASSIUM BROMIDE 3 [hp_X]/59mL
- POTASSIUM CHLORIDE 6 [hp_X]/59mL - A white crystal or crystalline powder used in BUFFERS; FERTILIZERS; and EXPLOSIVES. It can be used to replenish ELECTROLYTES and restore WATER-ELECTROLYTE BALANCE in treating HYPOKALEMIA.
- POTASSIUM IODIDE 3 [hp_X]/59mL - An inorganic compound that is used as a source of iodine in thyrotoxic crisis and in the preparation of thyrotoxic patients for thyroidectomy. (From Dorland, 27th ed)
- SODIUM BROMIDE 4 [hp_X]/59mL
- SULFUR IODIDE 14 [hp_X]/59mL
- SYZYGIUM JAMBOS SEED 14 [hp_X]/59mL
Which are Acne Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANTIMONY TRISULFIDE (UNII: F79059A38U)
- ANTIMONY TRISULFIDE (UNII: F79059A38U) (Active Moiety)
- ARSENIC TRIBROMIDE (UNII: 41CN475O7F)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- LYCOPERDON UTRIFORME FRUITING BODY (UNII: K2A74U428F)
- LYCOPERDON UTRIFORME FRUITING BODY (UNII: K2A74U428F) (Active Moiety)
- SYZYGIUM JAMBOS SEED (UNII: 97P0H45869)
- SYZYGIUM JAMBOS SEED (UNII: 97P0H45869) (Active Moiety)
- HYDROFLUORIC ACID (UNII: RGL5YE86CZ)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- POTASSIUM BROMIDE (UNII: OSD78555ZM)
- BROMIDE ION (UNII: 952902IX06) (Active Moiety)
- POTASSIUM IODIDE (UNII: 1C4QK22F9J)
- IODIDE ION (UNII: 09G4I6V86Q) (Active Moiety)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- SODIUM BROMIDE (UNII: LC1V549NOM)
- NICKEL SULFATE HEXAHYDRATE (UNII: JC9WZ4FK68)
- NICKEL CATION (UNII: OIS2CXW7AM) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- SULFUR IODIDE (UNII: L6L8KA2AA0)
- SULFUR IODIDE (UNII: L6L8KA2AA0) (Active Moiety)
Which are Acne Relief 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
Which are the Pharmacologic Classes for Acne Relief?
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Potassium Compounds - [CS]
- Potassium Salt - [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.
[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".