NDC 55146-005 5 Chronic Stress

Aralia Quinquefolia, Fucus Vesiculosus, Solidago Virgaurea, Taraxacum Officinale, Trifolium Pratense, Hydrastis Canadensis, Arsenicum Album, Calcarea Carbonica, Carbo Vegetabilis, Ceanothus Americanus, Cyclamen Europaeum, Hepar Sulphuris Calcareum, Natrum Muriaticum, Nux Vomica, Petroleum, Phosphorus

NDC Product Code 55146-005

NDC Code: 55146-005

Proprietary Name: 5 Chronic Stress 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: Aralia Quinquefolia, Fucus Vesiculosus, Solidago Virgaurea, Taraxacum Officinale, Trifolium Pratense, Hydrastis Canadensis, Arsenicum Album, Calcarea Carbonica, Carbo Vegetabilis, Ceanothus Americanus, Cyclamen Europaeum, Hepar Sulphuris Calcareum, Natrum Muriaticum, Nux Vomica, Petroleum, Phosphorus 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

  • 55146 - Biotics Research Corporation
    • 55146-005 - 5 Chronic Stress

NDC 55146-005-01

Package Description: 120 mL in 1 BOTTLE, PLASTIC

NDC Product Information

5 Chronic Stress with NDC 55146-005 is a a human over the counter drug product labeled by Biotics Research Corporation. The generic name of 5 Chronic Stress is aralia quinquefolia, fucus vesiculosus, solidago virgaurea, taraxacum officinale, trifolium pratense, hydrastis canadensis, arsenicum album, calcarea carbonica, carbo vegetabilis, ceanothus americanus, cyclamen europaeum, hepar sulphuris calcareum, natrum muriaticum, nux vomica, petroleum, phosphorus. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Biotics Research Corporation

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.

5 Chronic Stress 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.

  • AMERICAN GINSENG 3 [hp_X]/mL
  • FUCUS VESICULOSUS 3 [hp_X]/mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 3 [hp_X]/mL
  • TARAXACUM OFFICINALE 3 [hp_X]/mL
  • TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
  • GOLDENSEAL 5 [hp_X]/mL
  • ARSENIC TRIOXIDE 30 [hp_C]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_C]/mL
  • ACTIVATED CHARCOAL 30 [hp_C]/mL
  • CEANOTHUS AMERICANUS LEAF 30 [hp_C]/mL
  • CYCLAMEN PURPURASCENS TUBER 30 [hp_C]/mL
  • SODIUM CHLORIDE 30 [hp_C]/mL
  • STRYCHNOS NUX-VOMICA SEED 30 [hp_C]/mL
  • KEROSENE 30 [hp_C]/mL
  • PHOSPHORUS 30 [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)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

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: Biotics Research Corporation
Labeler Code: 55146
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: 06-11-2019 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: 12-31-2020 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.

5 Chronic Stress Product Label Images

5 Chronic Stress 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:

Aralia Quinquefolia 3X, 30C, Fucus Vesiculosus 3X, 30C, Solidago Virgaurea 3X, 30C, Taraxacum Officinale 3X, 30C, Trifolium Pratense 3X, 30C, Hydrastis Canadensis 5X, 30C, Arsenicum Album 30C, Calcarea Carbonica 30C, Carbo Vegetabilis 30C, Ceanothus Americanus 30C, Cyclamen Europaeum 30C, Hepar Sulphuris Calcareum 30C, Natrum Muriaticum 30C, Nux Vomica 30C, Petroleum30C, Phosphorus 30C

Indications:

For temporary relief of debility or exhaustion after slight exertion, or exhaustion following dysentery. Remedy #5 supports the easing of chronic stress produced by natural substances called adaptogens.

For temporary relief of debility or exhaustion after slight exertion, or exhaustion following dysentery. Remedy #5 supports the easing of chronic stress produced by natural substances called adaptogens.

Warnings:

If symptoms persist or worsen, seek the advice of a healthcare professional.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Caution: Not recommended for pregnant or lactating women.Tamper Seal: Sealed for your protection with a clear, full body seal. Do not use if seal is missing or broken.

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:

One (1) teaspoon twice daily or as directed by a healthcare professional. Consult a physician for use in children under 6 years of age.

Inactive Ingredients:

Citric Acid, Demineralized Water, Ethanol, Sodium Benzoate

Questions:

Distributed byBiotics Research CorporationRosenberg, TX 77471 • (281) 344-0909

Package Label Display:

Biotics Research Corporation's21st CENTURYHOMEOPATHICSNDC #55146-005-01HOMEOPATHIC REMEDY#5Chronic StressWater BasedFormula(2.85% Ethanol)4 fl. oz. (120ml)

* Please review the disclaimer below.

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