Instant Hand Sanitizer
FDA Label NDC 61010-2111

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Safetec Of America, Inc. for the product Instant Hand Sanitizer (NDC 61010-2111). 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 other, active ingredient, purpose, uses, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

Drug Facts

Active Ingredient

Ethyl Alcohol 66.5%

Purpose

Antiseptic

Uses

  • for handwashing to decrease bacteria on skin without soap and water
  • recommended for repeated use

Warnings

For external use only.

Flammable, keep away from fire or flame

Otc - Do Not Use

Do not use in the eyes. If this happens, rinse thoroughly with water

Otc - Stop Use

Stop use and ask doctor if irritation and redness develop and persists for more than 72 hours

Otc - Keep Out Of Reach Of Children

Keep out of reach of children If ingested get medical help or contact a Poison Control Center right away

Directions

  • wet hands and wrists thoroughly with product
  • allow to dry without wiping
  • children under 6 should be supervised while using this product

Inactive Ingredients

aloe vera, carbomer, fragrance, purified water, triethanolamine

Principal Display Panel – 64 Fl. Oz. Bottle

Safetec

NDC 61010-2111-7

instant

Hand

Sanitizer

Kills 99.9% of Germs

Enriched with
Aloe Vera

Citrus

Manufactured by
SAFETEC OF AMERICA, Inc.

Buffalo, NY 14215 800-456-7077 www.safetec.com

64 FL. OZ. (1.9 L) Reorder No. 18357

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