Keke Hand Sanitizer
FDA Label NDC 70415-511

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 Keke Hand Sanitizer (NDC 70415-511). 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 - when using, otc - keep out of reach of children, directions, other safety information, 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

ANTISEPTIC

Uses

  • TO DECREASE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE.
  • RECOMMEND FOR REPEATED USE.
  • USE ANYWHERE WITHOUT WATER.

Warnings

  • For external use only - hands.
  • Avoid eyes. In case of eye contact, flush with water.
  • Flammable. Keep away from fire or flame.
  • Discontinue if skin becomes irritated and ask a doctor.

Otc - When Using

When using this productavoid contact with eyes. In case of eye contact, flush with water

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.

Keep out of reach of children. In case of accidental ingestion seek professional assistance or contact a Poison Control Center immediately.

Directions

Wet hands thoroughly with product and rub until dry without wiping.

Other Safety Information

This product was not tested on animals.

Non Medicinal

ALCOHOL, AQUA, GLYCERIN, PROPYLENE GLYCOL, CARBOMER, AMINOMETHYL PROPANOL, PARFUM.

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