NDC 50181-0076 Candida Ease

Borax, Thuja Occidentalis, Arsenicum Album, Kreosotum, Sulphur, Candida Parapsilosis, Candida Albicans, Aspergillus Niger, Mucor Racemosus, Rhizopus Nigricans, Candida Krusei, Candida Tropicalis

NDC Product Code 50181-0076

NDC CODE: 50181-0076

Proprietary Name: Candida Ease What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Borax, Thuja Occidentalis, Arsenicum Album, Kreosotum, Sulphur, Candida Parapsilosis, Candida Albicans, Aspergillus Niger, Mucor Racemosus, Rhizopus Nigricans, Candida Krusei, Candida Tropicalis 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.

NDC Code Structure

  • 50181 - The Wellness Center For Research A

NDC 50181-0076-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Candida Ease with NDC 50181-0076 is a a human over the counter drug product labeled by The Wellness Center For Research A. The generic name of Candida Ease is borax, thuja occidentalis, arsenicum album, kreosotum, sulphur, candida parapsilosis, candida albicans, aspergillus niger, mucor racemosus, rhizopus nigricans, candida krusei, candida tropicalis. The product's dosage form is liquid and is administered via oral form.

Labeler Name: The Wellness Center For Research A

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug 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.

Candida Ease Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • SODIUM BORATE 3 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 3 [hp_X]/mL
  • ARSENIC TRIOXIDE 6 [hp_X]/mL
  • WOOD CREOSOTE 6 [hp_X]/mL
  • SULFUR 6 [hp_X]/mL
  • CANDIDA PARAPSILOSIS 12 [hp_X]/mL
  • CANDIDA ALBICANS 15 [hp_X]/mL
  • ASPERGILLUS NIGER VAR. NIGER 12 [hp_C]/mL
  • MUCOR RACEMOSUS 12 [hp_C]/mL
  • RHIZOPUS STOLONIFER 12 [hp_C]/mL
  • ISSATCHENKIA ORIENTALIS WHOLE 14 [hp_C]/mL
  • CANDIDA TROPICALIS 34 [hp_C]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: The Wellness Center For Research A
Labeler Code: 50181
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 05-04-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 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.

Exclude Flag: N - NO 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".

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Candida Ease Product Label Images

Candida Ease Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Borax 3X, Thuja Occidentalis 3X, 6X, Arsenicum Album 6X, 12X, 15X, 30X, 200X, Kreosotum 6X, 12X, 15X, 30X, 200X, Sulphur 6X, 12X, 15X, 30X, 200X, Candida Parapsilosis 12X, 15X, 30X, 200X, 6C, Candida Albicans 15X, 30X, 200X, 6C, Aspergillus Niger 12C, 15C, 30C, 100C, 200C, Mucor Racemosus 12C, 15C, 30C, 100C, 200C, Rhizopus Nigricans 12C, 32C, 34C, 55C, Candida Krusei 14C, 30C, 60C, Candida Tropicalis 34C, 55C, 89C.

Indications:

Indigestion, stomach swelling or distention, flatulence, edema, extreme tiredness, insomnia vaginal itching, vaginal soreness, vaginal discharge, brain-fog, lymph swelling, aches, pains, sniffles, runny nose.

Indigestion, stomach swelling or distention, flatulence, edema, extreme tiredness, insomnia vaginal itching, vaginal soreness, vaginal discharge, brain-fog, lymph swelling, aches, pains, sniffles, runny nose.

Warnings:

If pregnant or breast-feeding, ask a health professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.Store in a cool, dry place.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

5 drops two or three times per day on an empty stomach. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Organic Ethanol

Questons:

MFD FOR:The Wellness Center forResearch and Education, Inc.1237 S. Victoria Ave, Suite 169Oxnard, CA 93035www.wellnesscenter.net

Package Label Display:

Dr. Theresa Dale'sNDC: 50181-0076-1HomeopathicCANDIDA-EASE1 fl oz (30 ml)

* Please review the disclaimer below.