FDA Label for Dr. Butler Hemorrhoid Treatment

View Indications, Usage & Precautions

Dr. Butler Hemorrhoid Treatment Product Label

The following document was submitted to the FDA by the labeler of this product Beyond Health P.a.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Otc - Active Ingredient



Phenylephrine HCl 0.25%, Witch Hazel 50%


Otc - Purpose



Vasoconstrictor, Astringent


Indications & Usage



Temporarily reduces swelling associated with hemorrhoidal tissue. Temporary relief of anorectal itching and discomfort associated with hemorrhoids and other anorectal disorders.


Warnings



For external use only.

When using this product avoid spraying in eyes, contents under pressure. Do not puncture or incinerate. Do not store at temperatures above 120F, do not exceed recommended daily dosage unless directed by a doctor, do not put this product in the rectum by using fingers or any mechanical device or applicator.

Ask a doctor before use if you have heart disease, high blood pressure, thyroid disease, diabetes, difficulty in urination due to enlargement of the prostate gland, presently taking a prescription for high blood pressure or depression.

Stop use and ask a doctor if bleeding occurs, the condition worsens, symptoms last more than 7 days or clear up and occur again within a few days, needed for longer than 1 week.


Otc - Keep Out Of Reach Of Children



If swallowed, seek medical help or contact a Poison Control Center right away.


Inactive Ingredient



Alcohol 7%, Aloe Barbadensis Leaf Extract, Benzophenone-4, Disodium EDTA, Hydroxyethylcellulose, Methylparaben, Polysorbate 80, Propylene Glycol, Propylparaben, Sodium Citrate, Tocopheryl Acetate, Water.


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