Choctaw Hand Sanitizer
FDA Label NDC 75255-006

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Baoli Cosmetics Co., Ltd. for the product Choctaw Hand Sanitizer (NDC 75255-006). 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, otc - keep out of reach of children, warning, dosage & administration, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Alcohol 62% v/v

Purpose

 Antiseptic

Use

  • hand sanitizer to help reduce bacteria on the skin. For use when soap and water are not available.

Otc - Keep Out Of Reach Of Children

In case of accidental ingestion, contact a doctor or Poison Control Center immediately.

Warning

For external use only

Flammable, keep away from fire or flame.

When using this product

  • keep out of eyes, ears, and mouth.
  • In case of eye contact immediately flush eyes thoroughly with water.

    • Stop use and ask a doctor if

    • irritation or redness develops
    • conditions persist for more than 75 hours.

      • Other Information:

      • Store between 15-30 ℃ (59-86℉)
      • may discolor fabrics or surfaces

Dosage & Administration

  • Squeeze enough product on hands to cover all surfaces
  • rub hands together until dry
  • supervise children under 6 years of age when using this product to avoid swallowing.

Inactive Ingredients

Water, Carbomer, Aminomethyl Propanol

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