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Dch Rapid Relief Hemorrhoidal

Generic: Lidocaine 5%, Phenylephrine Hydrochloride 0.25%

OTC
Amides✓ FDA-verified
View full FDA label ↗
Dch Rapid Relief Hemorrhoidal is a spray that helps relieve itching and discomfort caused by issues around the anus, like hemorrhoids. It works by soothing the affected area to reduce irritation. For adults and children aged 12 and older, it should be applied externally up to 6 times a day, while children under 12 should consult a doctor before use. It's important to remember that this product is for external use only and should not be used near heat or flames. If you have heart disease, high blood pressure, or are taking medications for high blood pressure, it's best to talk to your doctor before using this medication.
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Uses

  • Local itching relief.
  • Discomfort from anorectal disorders.
  • Inflammation relief.
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Dosage

Cleanse the area with mild soap and warm water, then pat dry.
Adults and children 12 years and older: apply externally up to 6 times a day.
Children under 12 years: consult a doctor.
Wash hands after applying.
Always follow your doctor's specific instructions for your dose.
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Side effects

Common

Rectal bleeding may occurCondition may worsen or not improve within 7 daysRednessirritationswellingor pain may developSymptoms may increase

Serious

Allergic reactions to ingredients may happen
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Warnings

⚠ Important warnings

  • For external use only.
  • Flammable—do not use near heat or flame.
  • Avoid contact with eyes.
  • Do not puncture or incinerate.
  • Do not store above 120F.
  • Do not use fingers or devices to insert into the rectum.
  • Ask a doctor if you have heart disease, high blood pressure, thyroid disease, diabetes, or difficulty urinating.

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Answers pulled from the FDA label only.

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Medical Disclaimer: This content is provided for informational and educational purposes only and is not intended as medical advice. Always consult a qualified healthcare provider before taking any medication.
Data Source: Publicly available drug labeling information from the U.S. Food and Drug Administration (FDA).