Tucks Internal Soothers Hemorrhoidal

Tucks Internal Soothers Hemorrhoidal

Tucks Internal Soothers Hemorrhoidal Recall

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Questions & Answers

Side Effects & Adverse Reactions

For rectal use only

When using this product
  • do not use more than directed unless told to do so by a doctor
Stop use and ask a doctor if
  • rectal bleeding occurs
  • condition worsens or does not improve within 7 days

If pregnant or breastfeeding, ask a healthcare professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Stop use and ask a doctor if
  • rectal bleeding occurs
  • condition worsens or does not improve within 7 days

Legal Issues

There is currently no legal information available for this drug.

FDA Safety Alerts

There are currently no FDA safety alerts available for this drug.

Manufacturer Warnings

There is currently no manufacturer warning information available for this drug.

FDA Labeling Changes

There are currently no FDA labeling changes available for this drug.

Uses

  • temporary relieves these local symptoms associated with hemorrhoids and other anorectal disorders:
    • pain
    • itching
    • discomfort
  • temporarily forms a protective coating over inflamed tissues to help prevent drying of tissues
  • temporarily protects the inflamed, irritated anorectal surface to help make bowel movement less painful

History

There is currently no drug history available for this drug.

Other Information

There are no additional details available for this product.

Tucks Internal Soothers Hemorrhoidal Manufacturers


  • Mcneil-ppc, Inc.
    Tucks Internal Soothers Hemorrhoidal (Starch, Corn) Suppository [Mcneil-ppc, Inc.]

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