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Cold bee gone - Prescription Drug Labeling

Product NDC Code 70449-1000
Drug Name

Cold bee gone

Type Brand
Active Ingredients
Potassium dichromate 6 [hp_x]/ml
Schoenocaulon officinale seed 6 [hp_x]/ml
Luffa operculata fruit 6 [hp_x]/ml
Route NASAL
Dosage Form LIQUID
Labeler Name Buzzagogo, LLC
Packages
Package NDC Code Description
70449-1000-2 1 tube in 1 box (70449-1000-2) > 10 ml in 1 tube

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Kali Bichromicum 6X...Sinus congestion Sabadilla 6X...Sneezing, runny nose Luffa Operculata 6X...Post-nasal drip

Description

General information about the drug product, including the proprietary and established name of the drug, the type of dosage form and route of administration to which the label applies, qualitative and quantitative ingredient information, the pharmacologic or therapeutic class of the drug, and the chemical name and structural formula of the drug.
Overall Description

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Dosage & Administration Dosage and Administration

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Indications and Usage

Purpose

Information about the drug product’s indications for use.
Purpose Section

Spl product data elements

Usually a list of ingredients in a drug product.
Cold Bee Gone Kali Bichromicum 6X, Sabadilla 6X, Luffa Operculata 6X POTASSIUM DICHROMATE DICHROMATE ION LAVENDER OIL LIME OIL SCHOENOCAULON OFFICINALE SEED SCHOENOCAULON OFFICINALE SEED WATER ASCORBIC ACID LUFFA OPERCULATA FRUIT LUFFA OPERCULATA FRUIT HONEY

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Principal Display Panel Jar Label Jar Label

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Ask Doctor Section

Instructions for use

Information about safe handling and use of the drug product.
Box Insert Page 1 Box Insert Page 1 Box Insert Page 2 Box Insert Page 2

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children

Pregnancy or breast feeding

Pregnancy or Breast feeding
Pregnancy or Breast Feeding Section

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings Section

Disclaimer: Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API