Instant Hand Sanitizer
FDA Label NDC 25113-444

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dodge for the product Instant Hand Sanitizer (NDC 25113-444). 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 - do not use, otc - stop use, 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 Ingredient

Ethyl Alcohol 66.5%

Purpose

Antiseptic

Uses

  • for handwashing to decrease bacteria on skin
  • 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 a doctor if irritation and redness develop and persists for more than 72 hours

Keep Out Of Reach Of Children

If ingested get medical help or contact a Poison Control Center right away

Directions

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

Inactive Ingredients

aloe vera, carbomer, purified water, triethanolamine

Principal Display Panel - 59 Ml Bottle Label

NDC 25113-444-16

Dodge

quiksan®

Instant
Hand
Santizer

MEETS CDC HANDWASHING RECOMMENDATIONS

Kills 99.9% of Germs

Enriched with Aloe Vera

Unscented

2 fl oz (59mL)

Made in U.S.A.

Principal Display Panel (59 mL Bottle Label)

Principal Display Panel (59 mL Bottle Label)

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