Every Man Jack - Hand Sanitizer
FDA Label NDC 57934-5014

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Every Man Jack for the product Every Man Jack - Hand Sanitizer (NDC 57934-5014). 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 - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

ETHYL ALCOHOL 62%

Purpose

ANTISEPTIC

Uses

FOR HAND WASHING TO DECREASE BACTERIA ON SKIN.

Warnings

FOR EXTERNAL USE ONLY.

FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.

DO NOT USE IN EYES. IF CONTACT OCCURS, FLUSH THOROUGHLY WITH WATER. STOP USE AND ASK A DOCTOR IF REDNESS AND IRRITATION DEVELOP AND PERSISTS FOR MORE THAN 72 HOURS.

Otc - Keep Out Of Reach Of Children

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 AIR DRY.

Other Information

STORE AT ROOM TEMPERATURE. MAY DISCOLOR CERTAIN FABRICS.

Inactive Ingredients

PURIFIED WATER, GLYCERIN, CARBOMER, TRIETHANOLAMINE, TOCOPHERYL ACETATE, COCONUT OIL, CITRUS MEDICA (LEMON) PEEL OIL, ALOE VERA, FRAGRANCE

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