NDC 62106-1238 Anti-wart
Bufo Rana,Buxus Sempervirens,Juglans Regia,Nitricum Acidum,Oleander,Stannum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 62106-1238?
What are the uses for Anti-wart?
What are Anti-wart Active Ingredients?
- BUFO BUFO CUTANEOUS GLAND 12 [hp_X]/20mL
- BUXUS SEMPERVIRENS LEAFY TWIG 6 [hp_X]/20mL
- ENGLISH WALNUT 2 [hp_X]/20mL - A plant genus of the family JUGLANDACEAE that provides the familiar walnut.
- NERIUM OLEANDER LEAF 6 [hp_X]/20mL
- NITRIC ACID 10 [hp_X]/20mL - 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)
- SULFUR 10 [hp_X]/20mL - 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.
- TAXUS BACCATA WHOLE 6 [hp_X]/20mL
- THUJA OCCIDENTALIS LEAFY TWIG 8 [hp_X]/20mL
- TIN 10 [hp_X]/20mL - A trace element that is required in bone formation. It has the atomic symbol Sn, atomic number 50, and atomic weight 118.71.
- VANADIUM 10 [hp_X]/20mL - A metallic element with the atomic symbol V, atomic number 23, and atomic weight 50.94. It is used in the manufacture of vanadium steel. Prolonged exposure can lead to chronic intoxication caused by absorption usually via the lungs.
Which are Anti-wart UNII Codes?
The UNII codes for the active ingredients in this product are:
- TIN (UNII: 387GMG9FH5)
- TIN (UNII: 387GMG9FH5) (Active Moiety)
- ENGLISH WALNUT (UNII: 1V3SHR7QB7)
- ENGLISH WALNUT (UNII: 1V3SHR7QB7) (Active Moiety)
- NERIUM OLEANDER LEAF (UNII: 7KV510R6H6)
- NERIUM OLEANDER LEAF (UNII: 7KV510R6H6) (Active Moiety)
- BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q)
- BUFO BUFO CUTANEOUS GLAND (UNII: Q59QU6N72Q) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- VANADIUM (UNII: 00J9J9XKDE)
- VANADIUM (UNII: 00J9J9XKDE) (Active Moiety)
- BUXUS SEMPERVIRENS LEAFY TWIG (UNII: L479H0RS38)
- BUXUS SEMPERVIRENS LEAFY TWIG (UNII: L479H0RS38) (Active Moiety)
- TAXUS BACCATA WHOLE (UNII: T0311VH21D)
- TAXUS BACCATA WHOLE (UNII: T0311VH21D) (Active Moiety)
Which are Anti-wart 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
- LACTOSE (UNII: J2B2A4N98G)
Which are the Pharmacologic Classes for Anti-wart?
* 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".