Brazzers Anal Desensitizing Cream
FDA Label NDC 83553-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Metro Media Ent for the product Brazzers Anal Desensitizing (NDC 83553-001). 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, use (s), warnings:, do not use, keep out of reach of children., directions, other information:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Lidocaine 2%

Purpose

Anorectal

Use (S)

For temporary relief of pain, soreness or burning in the peritanal area.

Warnings:

For external use only.

Do Not Use

this product with a mechanical device. Certain persons can develop allergic reactions to 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. Do not apply onto cracked or broken skin. 

Keep Out Of Reach Of Children.

In case of any bleeding, discontinue use and consult a doctor. As with any drug, consult a health care professional.

Directions

Cleanse affected area with mild soap and water. Gently dry before application. Apply externally to the affected area up to 6 times daily.

Other Information:

  • Store at room temperture 68-77 °F (20-25 °C).
  • Do not use if temper evident seal on the outside of the container is broken or missing.

Inactive Ingredients:

Water, Dimethicone, Cetearyl Alcohol, Caprylic/Capric Triglyceride, Lidocaine, Glyceryl Stearate, Propylene Glycol, Ceteareth-20, 1,2-Hexanediol, Hydroxyacetophenone, Dimethiconal, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Xanthan Gum, Sodium Hydroxide.

Package Labeling:

Label (Label)

Label (Label)

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