NDC 44911-0013 Quercetin Phenolic

Quercetin,

NDC Product Code 44911-0013

NDC 44911-0013-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Quercetin Phenolic with NDC 44911-0013 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Quercetin Phenolic is quercetin, . 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 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.

Quercetin Phenolic 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.

  • QUERCETIN 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.
  • 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: 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: 06-05-2012 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: 12-31-2020 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.

Quercetin Phenolic Product Label Images

Quercetin Phenolic 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:  Quercetin 6X, 12X, 30X, 12C, 30C.

Otc - Purpose

INDICATIONS:  For temporary relief of symptoms of food and pollen sensitivities, fatigue, headache, runny nose and congestion, swelling, tendency to bruise easily, diarrhea, bloating and cramps.****These statements are based upon traditional homeopathic practice.  They have not been reviewed by the Food and Drug Administration.

Warnings

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.

Dosage & Administration

DIRECTIONS:  Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional.  If symptoms persist, consult your health care professional.  Consult a physician for use in children under 12 years of age.

Inactive Ingredient

INACTIVE INGREDIENTS:  Demineralized water, 20% Ethanol.

Otc - 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.

Indications & Usage

INDICATIONS:  For temporary relief of symptoms of food and pollen sensitivities, fatigue, headache, runny nose and congestion, swelling tendency to bruise easily, diarrhea, bloating and cramps.****These statements are based upon traditional homeopathic practice.  They have not been reviewed by the Food and Drug Administration.

Otc - Questions

Dist. by Energique, Inc.201 Apple Blvd.Woodbine, IA 51579800.869.8078

* Please review the disclaimer below.