NDC 55714-2400 Candida - Yeast

Adrenalinum, Candida Albicans, Thyroidinum, Torula Cerevisiae, Triticum, Ustilago Maidis, Antimon. Crud, Arsenicum Alb., Baptisia, Berber. Aqui., Bryonia, Calc. Phos., Cinchona, Helonias Dioica, Hydrastis, Iodium, Iris Versicolor, Kali Carb., Lachesis, Lycopodium, Merc. Viv., Nat.carb., Nat. Phos, Nitricum Ac., Phosphorus, Podoph. Pelt, Pulsatilla, Sepia, Echinacea, Ginkgo, Juglans Regia, Lappa, Thuja Occ.

NDC Product Code 55714-2400

NDC Code: 55714-2400

Proprietary Name: Candida - Yeast 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: Adrenalinum, Candida Albicans, Thyroidinum, Torula Cerevisiae, Triticum, Ustilago Maidis, Antimon. Crud, Arsenicum Alb., Baptisia, Berber. Aqui., Bryonia, Calc. Phos., Cinchona, Helonias Dioica, Hydrastis, Iodium, Iris Versicolor, Kali Carb., Lachesis, Lycopodium, Merc. Viv., Nat.carb., Nat. Phos, Nitricum Ac., Phosphorus, Podoph. Pelt, Pulsatilla, Sepia, Echinacea, Ginkgo, Juglans Regia, Lappa, Thuja Occ. 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

  • 55714 - Newton Laboratories, Inc.
    • 55714-2400 - Candida - Yeast

NDC 55714-2400-0

Package Description: 15 mL in 1 BOTTLE, GLASS

NDC 55714-2400-1

Package Description: 30 mL in 1 BOTTLE, GLASS

NDC 55714-2400-2

Package Description: 50 mL in 1 BOTTLE, GLASS

NDC Product Information

Candida - Yeast with NDC 55714-2400 is a a human over the counter drug product labeled by Newton Laboratories, Inc.. The generic name of Candida - Yeast is adrenalinum, candida albicans, thyroidinum, torula cerevisiae, triticum, ustilago maidis, antimon. crud, arsenicum alb., baptisia, berber. aqui., bryonia, calc. phos., cinchona, helonias dioica, hydrastis, iodium, iris versicolor, kali carb., lachesis, lycopodium, merc. viv., nat.carb., nat. phos, nitricum ac., phosphorus, podoph. pelt, pulsatilla, sepia, echinacea, ginkgo, juglans regia, lappa, thuja occ.. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Newton Laboratories, Inc.

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 - Yeast 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.

  • EPINEPHRINE 15 [hp_X]/mL
  • CANDIDA ALBICANS 15 [hp_X]/mL
  • THYROID, UNSPECIFIED 15 [hp_X]/mL
  • SACCHAROMYCES CEREVISIAE 15 [hp_X]/mL
  • ELYMUS REPENS ROOT 15 [hp_X]/mL
  • USTILAGO MAYDIS 15 [hp_X]/mL
  • ANTIMONY TRISULFIDE 10 [hp_X]/mL
  • ARSENIC TRIOXIDE 15 [hp_X]/mL
  • BAPTISIA TINCTORIA 10 [hp_X]/mL
  • MAHONIA AQUIFOLIUM ROOT BARK 10 [hp_X]/mL
  • BRYONIA ALBA ROOT 10 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 10 [hp_X]/mL
  • CINCHONA OFFICINALIS BARK 10 [hp_X]/mL
  • CHAMAELIRIUM LUTEUM ROOT 10 [hp_X]/mL
  • GOLDENSEAL 10 [hp_X]/mL
  • IODINE 10 [hp_X]/mL
  • IRIS VERSICOLOR ROOT 10 [hp_X]/mL
  • POTASSIUM CARBONATE 10 [hp_X]/mL
  • LACHESIS MUTA VENOM 10 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 10 [hp_X]/mL
  • MERCURY 10 [hp_X]/mL
  • SODIUM CARBONATE 10 [hp_X]/mL
  • SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 10 [hp_X]/mL
  • NITRIC ACID 10 [hp_X]/mL
  • PHOSPHORUS 10 [hp_X]/mL
  • PODOPHYLLUM 10 [hp_X]/mL
  • PULSATILLA VULGARIS 10 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 10 [hp_X]/mL
  • ECHINACEA, UNSPECIFIED 6 [hp_X]/mL
  • GINKGO 6 [hp_X]/mL
  • ENGLISH WALNUT 6 [hp_X]/mL
  • ARCTIUM LAPPA ROOT 6 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]/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.

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

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: Newton Laboratories, Inc.
Labeler Code: 55714
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: 11-06-2018 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: 12-31-2019 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Candida - Yeast Product Label Images

Candida - Yeast 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

Otc - Keep Out Of Reach Of Children Section

Keep out of reach of children.

Otc - Pregnancy Or Breast Feeding Section

If
pregnant or breast-feeding, ask a doctor before use.

Inactive Ingredient Section

USP Purified water; USP Gluten-free, non-GMO, organic cane alcohol 20%

Otc - Purpose Section

Formulated for associated symptoms such as gas, bloating, fatigue, mental fogginess, itching, discharge and other related symptoms.

Warnings Section

WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If
pregnant or breast-feeding, ask a doctor before use.

Questions Section

Newtonlabs.net - Questions? 800 448-7256Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013

Otc - Active Ingredient Section

Equal parts of Echinacea 6x, Ginkgo 6x, Juglans reg. 6x, Lappa 6x, Thuja occ. 6x, Antimon. crud. 10x, Baptisia 10x, Berber. aqui. 10x, Bryonia 10x, Calc. phos. 10x, Cinchona 10x, Helonias 10x, Hydrastis 10x, Iodium 10x, Iris vers. 10x, Kali carb. 10x, Lachesis 10x, Lycopodium 10x, Merc. viv. 10x, Nat.carb. 10x, Nat. phos. 10x, Nitricum ac. 10x, Phos. 10x, Podoph. pelt. 10x, Pulsatilla 10x, Sepia 10x, Adrenalinum 15x, Arsenium alb. 15x, Candida alb. 15x, Thyroidinum 15x, Torula cerevisiae 15x, Triticum 15x, Ustilago maidis 15x.

Dosage & Administration Section

Ages 12 and up, take 6 drops by mouth (ages 0 to 11, give 3 drops) one to four times daily or as directed by a health professional.Sensitive persons begin with 1 drop and gradually increase to full dose.

Indications & Usage Section

Formulated for associated symptoms such as gas, bloating, fatigue, mental fogginess, itching, discharge and other related symptoms.

* Please review the disclaimer below.

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