NDC 27281-008 Heartery

NDC Product Code 27281-008

NDC 27281-008-96

Package Description: 30 mL in 1 BOTTLE, SPRAY

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Heartery with NDC 27281-008 is a product labeled by Sunway Biotech Llc. The generic name of Heartery is . The product's dosage form is and is administered via form.

Labeler Name: Sunway Biotech Llc

Dosage Form: -

Product Type: 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.

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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Sunway Biotech Llc
Labeler Code: 27281
Start Marketing Date: 12-09-2013 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: I 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.

Heartery Product Label Images

Heartery 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: Aralia Quinquefolia 2X HPUS, Arnica Montana 3X HPUS, Aurum Metallicum 30C HPUS,Baryta Carbonica 30C HPUS, Belladonna 6X HPUS, Calcarea Fluorica 12x HPUS, Cholesterinum 30X HPUS, DNA 6X HPUS, Ginkgo Biloba 6X HPUS, RNA 6X HPUS, Viscum Album 3X HPUS, Zingiber Officinale 30C HPUS.

Otc - Purpose

NDC #: 2728100896HEARTERYEnergy Medicine with DNAHomeopathic Fast-Acting Oral Spray1.0 Fl. Oz. (30 mL)Alcohol 9% v/v

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Indications & Usage

Indications: Temporarily relieves symptoms associated with hypertension, such as: high blood pressure; constricted blood vessels; arteriosclerosis; inelastic blood vessels.

Dosage & Administration

Directions: Adults only: spray twice under the tongue, three times a day. This bottle contains about a 1 month supply.

Warnings

Warnings: Keep out of reach of children. If pregnant or breast feeding, ask a doctor before using product. Stop use and ask a doctor if symptoms persist more than 3 days, worsen, or new symptoms occur.

Other Safety Information

Tamper Evident Seal: Do not use if seal around neck of bottle is broken or missing. The letters HPUS indicate that ingredients are officially included in the Homeopathic Pharmacopoeia of the United States.Distributed by:SUNWAY BIOTECH, LLCOak Hills, CA 92344 U.S.A. info@sunwaybiotech.com

Inactive Ingredient

Inactive Ingredients: Alcohol 9% v/v, Glycerin 10% v/v, Purified Water.

* Please review the disclaimer below.