Dr. Easy Instant Hand Sanitizing Wipes
FDA Label NDC 52056-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dr. Easy Bio-tech (hefei) Co., Ltd. for the product Dr. Easy Instant Hand Sanitizing Wipes (NDC 52056-000). 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:, when using this product, stop use and ask a doctor, 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, 75%

Purpose

Antiseptic

Use

For sanitizing hands to decrease bacteria on the skin.

Warnings:

Flammable, keep away from fire or flame. For external use only.

When Using This Product

Keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

Stop Use And Ask A Doctor

If significant irritation, or sensitization develops. Consult a physician if irritation persists for more than 5 days

Keep Out Of Reach Of Children.

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

Directions

Peel back label at tab remove wipes as needed. reseal pouch by pressing label firmly back into place. wipe hands thoroughly with product.allow hands to air dry. Discard after single use.

Other Information

Do not store above 105F

Inactive Ingredients

Aloe barbadensis leaf juice (aloe vera), fragrance, glycerin, propylene glycol, water.

Package Labeling:

Label (Label)

Label (Label)

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