NDC 48951-1309 Argentum Malachite
Cream Topical - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 48951 - Uriel Pharmacy Inc.
- 48951-1309 - Argentum Malachite
Product Packages
NDC Code 48951-1309-5
Package Description: 60 g in 1 TUBE
Product Details
What is NDC 48951-1309?
What are the uses for Argentum Malachite?
What are Argentum Malachite Active Ingredients?
- AZADIRACHTA INDICA FLOWER 2 [hp_X]/g
- CUPRIC CATION 3 [hp_X]/g
- MERCURY 6 [hp_X]/g - A silver metallic element that exists as a liquid at room temperature. It has the atomic symbol Hg (from hydrargyrum, liquid silver), atomic number 80, and atomic weight 200.59. Mercury is used in many industrial applications and its salts have been employed therapeutically as purgatives, antisyphilitics, disinfectants, and astringents. It can be absorbed through the skin and mucous membranes which leads to MERCURY POISONING. Because of its toxicity, the clinical use of mercury and mercurials is diminishing.
- SILVER 3 [hp_X]/g - An element with the atomic symbol Ag, atomic number 47, and atomic weight 107.87. It is a soft metal that is used medically in surgical instruments, dental prostheses, and alloys. Long-continued use of silver salts can lead to a form of poisoning known as ARGYRIA.
Which are Argentum Malachite UNII Codes?
The UNII codes for the active ingredients in this product are:
- CUPRIC CATION (UNII: 8CBV67279L)
- CUPRIC CATION (UNII: 8CBV67279L) (Active Moiety)
- MERCURY (UNII: FXS1BY2PGL)
- MERCURY (UNII: FXS1BY2PGL) (Active Moiety)
- SILVER (UNII: 3M4G523W1G)
- SILVER (UNII: 3M4G523W1G) (Active Moiety)
- AZADIRACHTA INDICA FLOWER (UNII: 3TE8A92UPM)
- AZADIRACHTA INDICA FLOWER (UNII: 3TE8A92UPM) (Active Moiety)
Which are Argentum Malachite 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:
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- MINERAL OIL (UNII: T5L8T28FGP)
- WATER (UNII: 059QF0KO0R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POVIDONE-IODINE (UNII: 85H0HZU99M)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- SORBIC ACID (UNII: X045WJ989B)
- TEA TREE OIL (UNII: VIF565UC2G)
- POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
- XANTHAN GUM (UNII: TTV12P4NEE)
- FRANKINCENSE OIL (UNII: 67ZYA5T02K)
- MYRRH OIL (UNII: H74221J5J4)
- CITRUS PARADISI SEED (UNII: 12F08874Y7)
- ACETIC ACID (UNII: Q40Q9N063P)
- GLYCERIN (UNII: PDC6A3C0OX)
* 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".