NDC 44911-0039 Liquid B

Liquid B Homeopathic, Hordeum Vulgare, Hepar Suis, Heart (suis), Torula Cerevisiae

NDC Product Code 44911-0039

NDC 44911-0039-1

Package Description: 120 mL in 1 BOTTLE

NDC Product Information

Liquid B with NDC 44911-0039 is a a human prescription drug product labeled by Energique, Inc.. The generic name of Liquid B is liquid b homeopathic, hordeum vulgare, hepar suis, heart (suis), torula cerevisiae. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Energique, 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 Prescription 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.

Liquid B 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.

  • HORDEUM VULGARE TOP 2 [hp_X]/mL
  • PORK LIVER 6 [hp_X]/mL
  • PORK HEART 6 [hp_X]/mL
  • SACCHAROMYCES CEREVISIAE 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.

  • BIOTIN (UNII: 6SO6U10H04)
  • CHOLINE BITARTRATE (UNII: 6K2W7T9V6Y)
  • ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
  • FRUCTOSE (UNII: 6YSS42VSEV)
  • CYANOCOBALAMIN (UNII: P6YC3EG204)
  • CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
  • ALCOHOL (UNII: 3K9958V90M)
  • FOLIC ACID (UNII: 935E97BOY8)
  • CITRUS PARADISI SEED (UNII: 12F08874Y7)
  • INOSITOL (UNII: 4L6452S749)
  • SIRAITIA GROSVENORII FRUIT (UNII: NOU2FB51TW)
  • ORANGE (UNII: 5EVU04N5QU)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • NIACINAMIDE (UNII: 25X51I8RD4)
  • AMINOBENZOIC ACID (UNII: TL2TJE8QTX)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
  • RIBOFLAVIN (UNII: TLM2976OFR)
  • THIAMINE HYDROCHLORIDE (UNII: M572600E5P)
  • XANTHAN GUM (UNII: TTV12P4NEE)

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

Pharmacological Class(es)

What is a Pharmacological Class?
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

  • Non-Standardized Fungal Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Allergens - [CS]
  • Fungal Proteins - [CS]
  • Non-Standardized Fungal Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Dietary Proteins - [CS]
  • Allergens - [CS]
  • Fungal Proteins - [CS]

Product Labeler Information

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

Labeler Name: Energique, Inc.
Labeler Code: 44911
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: 10-29-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 08-02-2023 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

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.

Liquid B Product Label Images

Liquid B 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

Liquid B Homeopathic, Hordeum Vulgare 2X, Hepar Suis 6X, Heart (Suis) 6X, Torula Cerevisiae 6X

Indications

For temporary relief of pellagra and vasoconstriction.

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. Store in a cool, dry place.

Directions

Adults: 1 to 2 teaspoons per day. Children under 9 years of age: 1/2 teaspoon per day or as directed by a health care professional. Shake well before use. Consult a physician for use in children under 12 years of age.

Inactive Ingredients

Biotine, Choline Bitartrate, Citric Acid, Crystalline Fructose, Cyanocobalamin, D-Calcium Pantothenate, Demineralized Water, Ethanol, Folic Acid, Grapefruit Seed Extract, Inositol, Lo Han Fruit Concentrate, Natural Flavor Blend and/or other Natural Juice Concentrates and Natural Flavors, Natural Vegetable Glycerin, Niacimamide, Para aminobenzoic Acid, Potassium Sorbate, Pyridoxine Hydrochloide, Riboflavin, Thiamin Hydrochloride, Xanthan Gum.

Keep Out Of Reach Of Children

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

Indications And Usage

For temporary relief of pellagra and vasoconstriction.

Questions

Dist. by Energique, Inc.201 Apple BlvdWoodbine, IA 51579800-869-8078

* Please review the disclaimer below.