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Umcka fastactives cherry - Medication Information

Product NDC Code 83102-1166
Drug Name

Umcka fastactives cherry

Type Brand
Active Ingredients
Pelargonium sidoides root 1 [hp_x]/700mg
Route ORAL
Dosage Form POWDER
Labeler Name ProSolutions Inc.
Packages
Package NDC Code Description
83102-1166-0 10 packet in 1 carton (83102-1166-0) / 700 mg in 1 packet
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Overdosage of Umcka FastActives Cherry

Information about signs, symptoms, and laboratory findings of acute ovedosage and the general principles of overdose treatment.
Over dosage Over dosage panel.

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients

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 panel

Inactive ingredient

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

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 panel Indications and Usage panel

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Umcka FastActives Cherry Pelargonium sidoides SILICON DIOXIDE XYLITOL MALTODEXTRIN PELARGONIUM SIDOIDES ROOT PELARGONIUM SIDOIDES ROOT CITRIC ACID MONOHYDRATE MALIC ACID Natural Cherry Flavor

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.
Package panel Package panel

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 a Doctor panel Ask a Doctor panel

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. Keep out of reach of children.

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop Use panel Stop Use panel

Pregnancy or breast feeding

Pregnancy or Breast feeding
Pregnancy or Breast Feeding panel Pregnancy or Breast Feeding panel

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 panel Warnings panel

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me 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