Eunos
FDA Label NDC 75007-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Yirong Trading (nanjing) Co., Ltd for the product Eunos (NDC 75007-002). 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, inactive ingredients, package label - principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 75% v/v.

Purpose

Antimicrobial

Uses

Hand Sanitizer to help reduce bacteria on the skin that potentially can cause disease. 

Warnings

Flammable. Keep away from fire or flame.

For external use only.

When using this product

  • do not use in or near the eyes. In case of contact with eyes, rinse eyes thoroughly with water.
  • avoid using on broken skin.

    • 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 enough product 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.

Inactive Ingredients

Aqua, Glycerin, Propylene Glycol, Carbomer, Aminomethyl Propanol, Aloe Barbadensis (Aloe Vera) Gel, Tocopheryl Acetate (Vitamin E)

Package Label - Principal Display Panel

500 mL Label

1000 mL Label

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