NDC 57520-0417 Cystotone

NDC Product Code 57520-0417

NDC CODE: 57520-0417

Proprietary Name: Cystotone What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

  • 57520 - Apotheca Company

NDC 57520-0417-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

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

NDC Product Information

Cystotone Product Label Images

Cystotone 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:  Sarsaparilla 3X, Uva-ursi 3X, Arsenicum album 12X, Cantharis 12X, Pareira brava 12X, Pulsatilla 12X, Sepia 12X, Terebinthina 12X, Populus tremuloides 15X.

Otc - Purpose

INDICATIONS:  For temporary relief of intolerable urging and tenesmus, pressure in the area of the bladder, urination often.


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

SUGGESTED USE:  Adults and children 5 to 10 drops orally, 3 times 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 - Questions

Dist. By:Energique, Inc.201 Apple Blvd.Woodbine, IA 51579800-869-8078

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