Dr. Palm Hand Sanitizer
FDA Label NDC 81236-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Skinnydip Limited for the product Dr. Palm Hand Sanitizer (NDC 81236-001). 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, uses, warnings, directions, keep out of reach of children., inactive ingredients., other information., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Alcohol 75%

Purpose

Antiseptic

Uses

  • Hand sanitizer to help reduce bacteria on the skin that could cause disease.
  • For use when soap and water are not available

Warnings

For external use only. Flammable. Keep away from heat or flame.

  • Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

    • Do not use 

    • in children less than 2 months of age.
    • on open skin wounds.

      • When using this product

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

Directions

  • Place enough product in your hands to cover all surfaces. 
  • Rub hands together until dry.
  • Supervise children under 6 years of age when  using this product to avoid swallowing.

Keep Out Of Reach Of Children.

  •  If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Inactive Ingredients.

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Extract, Aminomethyl Propanol,Butylene Glycol, Glycerin, Water (Aqua).

Other Information.

• Store between 15-30°C (59-86°F)
• Avoid freezing and excessive heat above 40°C(104°F)

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