Foasu Daily Hand Sanitizer Gel
FDA Label NDC 77964-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Hanscos Co.,ltd. for the product Foasu Daily Hand Sanitizer Gel (NDC 77964-001). 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, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, 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%

Purpose

Antimicrobial

Use

  • Hand sanitizer to help reduce bacteria on the skin

Warnings

Flammable. Keep away from fire or flame.

For external use only

Otc - When Using

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

Otc - Stop Use

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

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.

Directions

  • Put nough produt in your palm to cover hands and rub hands together briskly until dry.
  • Children under 6 years of age should be supervised when using this product

Other Information

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

Inactive Ingredients

WATER, GLYCERIN, PEG-60 HYDROGENATED CASTOR OIL, CARBOMER, TRIETHANOLAMINE, CAMELLIA SIMENSIS LEAF EXTRACT, ALOE BARBADENSIS LEAF EXTRACT, MENTHA PIPERITA (PEPPERMINT) OIL, LIMONENE

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