Acne Face And Body Shampoo, Suspension
FDA Label NDC 70707-101

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Face Reality, Inc. for the product Acne Face And Body (NDC 70707-101). 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, do not use, 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

Benzoyl Peroxide 2.5%

Purpose

For the treatment of Acne

Uses

Adults and children 12 years and over:

  • For the treatment of acne.
  • For acne-prone or oily skin.

Warnings

FOR EXTERNAL USE ONLY. Avoid contact with eyes and eyelids. This product may cause irritation. Mild irritation may be reduced by using the product less frequently. If irritation becomes severe, discontinue use and consult a doctor.

Do Not Use

this medication if you have very sensitive skin or if you are sensitive to benzoly peroxide.

Directions

Use 1 to 3 times daily on affected skin, work into lather, rinse off thoroughly.

Other Information

May bleach hair or fabrics. Store at room temperature. Keep away from heat or direct sunlight.

Inactive Ingredients

Purified Water, Ammonium Lauryl Sulfate, Glycerin, Cellulose Acetate, Disodium Cocoamphodiacetate, Propylene Glycol, Carbomer, Sodium Hydroxide, Fragrance.

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