Go Care Advanced Hand Sanitizer
FDA Label NDC 79110-141

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Global Genesis Partners Llc for the product Go Care Advanced Hand Sanitizer (NDC 79110-141). 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 drug facts, active ingredient, purpose, warnings, otc - keep out of reach of children, other information, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Warnings

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

When using this product do not use in or near eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

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

Otc - Keep Out Of Reach Of Children

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

Other Information

  • Store below 110°F (43°C).
  • May discolor certain fabrics or surfaces.

Inactive Ingredients

Water, Glycerin, Squalane, Panthenol, Inulin, Sodium Hyaluronate, Fructose, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol.

Packaging

Image (7911014102 25)

Image (7911014102 25)

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