Rite Aid Renewal
FDA Label NDC 11822-2683

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Rite Aid Corporation for the product Rite Aid Renewal (NDC 11822-2683). 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, keep out of reach of children, directions, other information, questions or comments?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

ETHYL ALCOHOL 62%

Purpose

ANTISEPTIC

Uses

TO HELP REDUCE BACTERIA ON THE SKIN

Warnings

FOR EXTERNAL USE ONLY. FLAMMABLE. KEEP AWAY FROM SOURCES OF HEAT AND FIRE.

Keep Out Of Reach Of Children

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

Directions

WET HANDS THOROUGHLY AND RUN TOGETHER UNTIL DRY.

Other Information

STORE AT A TEMPERATURE BELOW 110F.

Questions Or Comments?

1-866-695-3030

Inactive Ingredients

WATER (AQUA), GLYCERIN, ISOPROPYL MYRISTATE, PROPYLENE GLYCOL, TOCOPHERYL ACETATE, AMINOMETHYL PROPANOL, CARBOMER, FRAGRANCE (PARFUM).

Label Copy

Image Of The Label (17410l)

Image Of The Label (17410l)

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