Body Action Products Butt Eze Benzocaine Gel
FDA Label NDC 70742-286

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Product Max Group Inc for the product Body Action Products Butt Eze Benzocaine (NDC 70742-286). 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, keep out of reach of children., directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Benzocaine 5%

Purpose

Anorectal (Hemorrhoidal) Gel

Uses

  • For temporary relief of pain or soreness in the perianal area.

Warnings

For external use only.

  • Avoid contact with the eyes.
  • Certain persons can develop allergic reactions from ingredients in this product. If the symptom being treated does not subside or if redness, irritation, swelling, pain or other symptoms develop or increase, discontinue use and consult a doctor.

Keep Out Of Reach Of Children.

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

Directions

  • When practial, cleanse the affected area with mild soap and warm water and rinse thoroughly.
  • Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product.
  • Apply to the affected area up to 6 times daily.

Other Information

Do not use if safety seal is broken or missing.

Inactive Ingredients

Cannabis Sativa (Hemp) Seed Oil, Hydroxyethylcellulose, Methylparaben, PEG-8, Polysorbate 20, Propylene Glycol, Propylparaben, Water.

Package Labeling:

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