NDC 43742-1202 Candida Spp
Alternaria Tenuis Nees,Aspergillus Niger,Candida Albicans,Candida Parapsilosis,Mucor - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-1202 - Candida Spp
Product Packages
NDC Code 43742-1202-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-1202?
What are the uses for Candida Spp?
What are Candida Spp Active Ingredients?
- ALTERNARIA ALTERNATA 12 [hp_X]/mL
- ASPERGILLUS NIGER VAR. NIGER 12 [hp_X]/mL
- AUREOBASIDIUM PULLULANS VAR. PULLUTANS 12 [hp_X]/mL
- CANDIDA ALBICANS 12 [hp_X]/mL - A unicellular budding fungus which is the principal pathogenic species causing CANDIDIASIS (moniliasis).
- CANDIDA PARAPSILOSIS 12 [hp_X]/mL - A species of MITOSPORIC FUNGI and opportunistic pathogen associated with its ability to form BIOFILMS in catheters and parenteral nutrition IV lines. C. parapsilosis complex includes closely related species C. orthopsilosis; and C. metapsilosis.
- CANDIDA TROPICALIS 31 [hp_C]/mL - A species of MITOSPORIC FUNGI that is a major cause of SEPTICEMIA and disseminated CANDIDIASIS, especially in patients with LYMPHOMA; LEUKEMIA; and DIABETES MELLITUS. It is also found as part of the normal human mucocutaneous flora.
- ISSATCHENKIA ORIENTALIS WHOLE 15 [hp_C]/mL
- MUCOR RACEMOSUS 12 [hp_X]/mL
- RHIZOPUS STOLONIFER 12 [hp_X]/mL
- SACCHAROMYCES CEREVISIAE 12 [hp_X]/mL - A species of the genus SACCHAROMYCES, family Saccharomycetaceae, order Saccharomycetales, known as "baker's" or "brewer's" yeast. The dried form is used as a dietary supplement.
Which are Candida Spp UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H)
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (Active Moiety)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6)
- ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (Active Moiety)
- CANDIDA ALBICANS (UNII: 4D7G21HDBC)
- CANDIDA ALBICANS (UNII: 4D7G21HDBC) (Active Moiety)
- CANDIDA PARAPSILOSIS (UNII: 0KZ676D44N)
- CANDIDA PARAPSILOSIS (UNII: 0KZ676D44N) (Active Moiety)
- MUCOR RACEMOSUS (UNII: 17RH99LQ7G)
- MUCOR RACEMOSUS (UNII: 17RH99LQ7G) (Active Moiety)
- AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK)
- AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK) (Active Moiety)
- RHIZOPUS STOLONIFER (UNII: FEE198DK4Q)
- RHIZOPUS STOLONIFER (UNII: FEE198DK4Q) (Active Moiety)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H) (Active Moiety)
- ISSATCHENKIA ORIENTALIS WHOLE (UNII: 138TJ2U1SD)
- ISSATCHENKIA ORIENTALIS WHOLE (UNII: 138TJ2U1SD) (Active Moiety)
- CANDIDA TROPICALIS (UNII: Q222J2186W)
- CANDIDA TROPICALIS (UNII: Q222J2186W) (Active Moiety)
Which are Candida Spp 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Candida Spp?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Fungal Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Fungal Allergenic Extract - [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.
[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".