NDC 54118-7990 Gyne - Tox

Adrenal, Angelica Atropurpurea, Boricum Acidum, Atp

NDC Product Code 54118-7990

NDC 54118-7990-2

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Gyne - Tox with NDC 54118-7990 is a a human over the counter drug product labeled by Abco Laboratories, Inc.. The generic name of Gyne - Tox is adrenal, angelica atropurpurea, boricum acidum, atp. The product's dosage form is solution/ drops and is administered via oral form.

Labeler Name: Abco Laboratories, Inc.

Dosage Form: Solution/ Drops - A solution which is usually administered in a drop-wise fashion.

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.

Gyne - Tox 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.

  • BOS TAURUS ADRENAL GLAND 6 [hp_X]/60mL
  • ANGELICA ATROPURPUREA ROOT 3 [hp_X]/60mL
  • BORIC ACID 12 [hp_X]/60mL
  • ADENOSINE TRIPHOSPHATE 5 [hp_X]/60mL
  • BOS TAURUS MESENCHYME 6 [hp_X]/60mL
  • CANDIDA ALBICANS 6 [hp_X]/60mL
  • BLACK COHOSH 3 [hp_X]/60mL
  • WOOD CREOSOTE 12 [hp_X]/60mL
  • BOS TAURUS LYMPH 6 [hp_X]/60mL
  • GONORRHEAL URETHRAL SECRETION HUMAN 30 [hp_X]/60mL
  • MERCURIUS SOLUBILIS 12 [hp_X]/60mL
  • ESTRONE 30 [hp_X]/60mL
  • BOS TAURUS OVARY 5 [hp_X]/60mL
  • BOS TAURUS PLACENTA 5 [hp_X]/60mL
  • SCABIES LESION LYSATE (HUMAN) 30 [hp_X]/60mL
  • ANEMONE NEMOROSA 12 [hp_X]/60mL
  • SEPIA OFFICINALIS JUICE 12 [hp_X]/60mL
  • DELPHINIUM STAPHISAGRIA SEED 12 [hp_X]/60mL
  • TREPONEMIC SKIN CANKER HUMAN 30 [hp_X]/60mL
  • THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/60mL
  • THYROID, UNSPECIFIED 6 [hp_X]/60mL
  • BOS TAURUS UTERUS 5 [hp_X]/60mL

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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • 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: Abco Laboratories, Inc.
Labeler Code: 54118
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: 12-19-2012 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: 12-31-2017 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: E 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.

Gyne - Tox Product Label Images

Gyne - Tox 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 - Active Ingredient

  • Active Ingredients:Adrenal 6xAngelica atropurpurea 3xBoricum acidum 12xATP 5xMesenchyme 6x, 9x, 6cCandida albicans 6x, 12x, 30xCimicifuga racemosa 3xKreosotum 12xLymph 6xMedorrhinum 30xMercurius solubilis 12xFemale nosode 30x, 6x, 100xOvary 5xPlacenta 5xPsorinum 30xPulsatilla nigricans 12xSepia 12xStaphysagria 12xSyphilinum 30xThuja occidentalis 12xThyroid 6xUterus 5x

Otc - Purpose

  • Homeopathic Relief of Female Toxin Sensitivity Symptoms

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children

Indications & Usage

  • 30 drops 2X daily or as recommended by a health care practitionerShake well before use

Warnings

  • If you are pregnant, breastfeeding or taking medications consult a health care practitioner before use. Keep out of reach of childrenDo not use if seal is missing or broken

Dosage & Administration

  • 30 drops 2X daily or as recommended by a health care practitionerShake well before use

Inactive Ingredient

  • Reverse osmosis waterVegetabe glycerinAlcohol (ethanol)

* Please review the disclaimer below.

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