Fresh Hand Foaming Hand Sanitizer Alcohol Foam
FDA Label NDC 70415-203

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cwgc La Inc. for the product Fresh Hand Foaming Hand Sanitizer Alcohol Foam (NDC 70415-203). 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, when using this product, keep out of reach of children., otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Ethyl Alcohol 70 %

Purpose

Antibacterial

ANTIBACTERIAL

Uses

  • Hand sanitizer to help reduce bacteria on the skin.

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, rinse eyes thoroughly with water.

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

When Using This Product

  • avoid contact with eyes. In case of eye contact, flush with water

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

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

  • Place enough product on your palm to thoroughly cover your hands
  • Rub hands together briskly until dry

Inactive Ingredients

Water, Isopropyl Alcohol, Propylene Glycol, PEG-12 Dimethicone Crosspolymer, BIS-PEG-12 Dimethicone.

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