Hand Sanitizer
FDA Label NDC 58037-102

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Pride Products Corp. for the product Hand Sanitizer (NDC 58037-102). 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, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

ETHYL ALCOHOL 62.0%

Purpose

ANTIMICROBIAL

Uses

HAND SANITIZER TO HELP REDUCE BACTERIA ON THE SKIN

Warnings

FOR EXTERNAL USE ONLY

FLAMMABLE. KEEP AWAY FROM HEAT AND FLAME.

WHEN USING THIS PRODUCT AVOID CONTACT WITH FACE, EYES, AND BROKEN SKIN. IN CASE OF EYE CONTACT, FLUSH WITH PLENTY OF WATER AND SEEK MEDICAL ADVICE.

STOP USE AND ASK A DOCTOR IF IRRITATION OR REDNESS DEVELOPS.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.

Directions

  • WET HANDS THOROUGHLY WITH PRODUCT AND RUB INTO SKIN UNTIL DRY.
  • CHILDREN UNDER 6 YEARS OF AGE SHOULD BE SUPERVISED BY AN ADULT WHEN USING THIS PRODUCT.

Inactive Ingredients

WATER (AQUA), ALOE BARBADENSIS LEAF JUICE, CARBOMER, FRAGRANCE, GLYCERIN, PROPYLENE GLYCOL, TOCOPHERYL ACETATE (VITAMIN E), TRIETHANOLAMINE, FD&C BLUE NO. 1, FD&C YELLOW NO. 5.

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