Hand Sanitizer
FDA Label NDC 75887-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Aztex Enterprises for the product Hand Sanitizer (NDC 75887-001). 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 otc - keep out of reach of children, otc - purpose, warnings, indications & usage, inactive ingredient, otc - active ingredient, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Keep Out Of Reach Of Children

Flammable, keep away from fire or flames.Keep out of reach of childrenIf swallowed contact a Poison Control Center right awayIf pregnant or breast feeding, ask a health care professional before use

Otc - Purpose

Usesfor handwashing to decrease bacteria on the skin.

Warnings

Warnings for external use only.When using this product; Do not use in eyes.Discontinue use if irritation and redness develop

Indications & Usage

Directionswet hand thoroughly with productbriskly rub hands together until dry

Inactive Ingredient

Inactive IngredientsDeionized waterGlycerinPropylen GlycolTriethanolamineCarbomerMethyloarabenProplyparabenLemon Fragrance

Otc - Active Ingredient

Drug Fact 8ml/0.25 fl.oz. Made in Canada -> (L) 8295Active ingredient PurposeEthyl alcohol 62% Antisepctic

Dosage & Administration

8ml/0.25 fl. oz.

Package Label.Principal Display Panel

Anticeptic Hand SanitizerAZX SPORTManufactured forAZX SPORT925 Century DriveBurlington, ON L7L 5LB

* Please review the disclaimer below.