Hemorrhoidal Pads Patch
FDA Label NDC 41250-868

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Meijer Distribution Inc. for the product Hemorrhoidal Pads (NDC 41250-868). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

When Using This Product

  • do not exceed the recommended daily dosage unless directed by a doctor.
  • do not insert into rectum or vagina using fingers or mechanical device.

Stop Use And Ask A Doctor If

  • rectal bleeding occurs
  • condition worsens or does not improve within 7 days.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Other Information

Store at controlled room temperature: 15°-30°C (59°-86°F)

Other Safety Information

Do not use this product if seal on jar is broken or missing.

Other

* This product is not manufactured or distributed by Blistex, Inc., owner of the registered trademark TUCKS®.

* Please review the disclaimer below.