Hand Sanitizer Gel
FDA Label NDC 70412-194

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Ayan Biotech Co.,ltd. for the product Hand Sanitizer (NDC 70412-194). 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 ingredients, purpose, uses, 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.

Label Section Quick Index

Active Ingredients

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

For Hand Sanitizing

Warnings

For external use only-hands.

Flammable.Keep away from heat and flame.

When Using This Product

  • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • Avoid contact with broken skin.
  • Do not inhale or ingest.

Stop Use And Ask A Doctor

  • if skin irritation or develops.

Keep Out Of Reach Of Children.

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

Directions

  • Wet hands thoroughly with product and allow to dry without wiping.
  • For children under 6 use only under adult Supervision
  • Not recommender for infants

Other Information

  • Do not store above 105°F.
  • May discolor some fabrics.
  • Harmful to wood finishes and plastics.

Inactive Ingredients

Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water.

Package Labeling:

Label3 (Label3)

Label3 (Label3)

Package Labeling: 15Ml

Label4 (Label4)

Label4 (Label4)

Package Labeling: 53Ml

Label5 (Label5)

Label5 (Label5)

Package Labeling: 60Ml

Label6 (Label6)

Label6 (Label6)

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