Pure X Alcohol Wipes
FDA Label NDC 80671-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Quanzhou Aiwina Hygiene Products Co.,ltd for the product Pure X Alcohol Wipes (NDC 80671-002). 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 drug facts, active ingredients, purpose, indication and usage, warnings, otc - keep out of reach of children, directions of use, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredients

Ethyl Alcohol 75%

Purpose

Antiseptic

Indication And Usage

  • For hand washing in order to sanitize skin  (hands must air dry)

Warnings

  • For external use only.
  • Keep out of reach of eyes. If contact occurs, rinse thoroughly with water.
  • Do not use if you are allergic to any of the ingredients.
  • Discontinue use if irritation or redness develops, and if condition persists for more than 72 hours consult a physician.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children unless under adult supervision.
  • If swallowed, get medical help.

Directions Of Use

  • Wet hands thoroughly with product and allow to dry without rinse.
  • Children under six years of age should be supervised when using this product.

Other Information

  • Store in a dry place away from fire.

Inactive Ingredients

  • Purified (RO) Water, Aloe Vera Extract

Packaging

Image (8067100210)

Image (8067100210)

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