NDC 61657-0101 Cand-ex
Lycopodium, Nux Vomica, Borax, Asafoetida, Nux Moschata, Gentiana Lutea, Kreosotum, - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61657 - White Manufacturing Inc. Dba Micro West
- 61657-0101 - Cand-ex
Product Packages
NDC Code 61657-0101-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 61657-0101?
What are the uses for Cand-ex?
What are Cand-ex Active Ingredients?
- ASAFETIDA 12 [hp_X]/30mL - A plant genus of the family APIACEAE. It contains pungent oils and resins. It is used to flavor curries, as a carminative, and as cat and dog repellent. The occasionally used common name of 'giant fennel' should not be confused with true fennel (FOENICULUM).
- BAPTISIA TINCTORIA 3 [hp_X]/30mL
- ECHINACEA, UNSPECIFIED 3 [hp_X]/30mL
- GENTIANA LUTEA ROOT 3 [hp_X]/30mL
- LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/30mL
- NUTMEG 12 [hp_X]/30mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/30mL
- PHOSPHORIC ACID 12 [hp_X]/30mL
- PULSATILLA VULGARIS 30 [hp_X]/30mL
- SEPIA OFFICINALIS JUICE 30 [hp_X]/30mL
- SODIUM BORATE 12 [hp_X]/30mL
- STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/30mL
- WOOD CREOSOTE 12 [hp_X]/30mL
Which are Cand-ex UNII Codes?
The UNII codes for the active ingredients in this product are:
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX)
- ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (Active Moiety)
- BAPTISIA TINCTORIA (UNII: 5K1UO2888Y)
- BAPTISIA TINCTORIA (UNII: 5K1UO2888Y) (Active Moiety)
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- WOOD CREOSOTE (UNII: 3JYG22FD73)
- WOOD CREOSOTE (UNII: 3JYG22FD73) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- BORATE ION (UNII: 44OAE30D22) (Active Moiety)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS) (Active Moiety)
- NUTMEG (UNII: AEE24M3MQ9)
- NUTMEG (UNII: AEE24M3MQ9) (Active Moiety)
- ASAFETIDA (UNII: W9FZA51AS1)
- ASAFETIDA (UNII: W9FZA51AS1) (Active Moiety)
Which are Cand-ex 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)
Which are the Pharmacologic Classes for Cand-ex?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Food Additives - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- 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".