Kleanops
FDA Label NDC 79912-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Kleanops Llc for the product Kleanops (NDC 79912-001). 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, otc - 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

Ethyl Alcohol 70% v/v.

Purpose

Antiseptic

Uses

To decrease bacteria on skin.

Warnings

For external use only.

Flammable. Keep away from heat or flame.

Do not use
• On open skin wound.
• On children less than 2 months of age.

When using this product keep out of eyes. In case of contact, rinse eyes with water.

Stop use and ask a doctor if irritation or rash appears.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

  • Wipe hands thoroughly with product and allow to dry.
  • Children under 6 years of age must be supervised when using this product.

Other Information


• Store below 40°C (104°F).
• May discolor certain fabric.

Inactive Ingredients

Water (Aqua), Aloe Barbadensis Leaf Juice, Glycerin, Isopropyl Myristate, Tocopheryl Acetate

Package Label - Principal Display Panel

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