One Step Wipes
FDA Label NDC 60742-200

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Belvedere International Inc. for the product One Step Wipes (NDC 60742-200). 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 package label.principal display panel, active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Package Label.Principal Display Panel

DRUG FACTS

Active Ingredient

Ethyl Alcohol 62%

Otc - Purpose

USE ANYTIME FOR QUICK CLEAN UP WHEN SOAP AND WATER ARE NOT AVAILABLE

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Indications & Usage

USE ANYTIME FOR QUICK CLEAN UP WHEN SOAP AND WATER ARE NOT AVAILABLE

Warnings

FOR EXTERNAL USE ONLY, KEEP OUT OF REACH OF CHILDREN, FLAMMABLE, KEEP AWAY FROM OPEN FLAME AND SOURCES OF HEAT. AVOID CONTACT WITH EYES SHOULD THIS OCCUR FLUSH EYES WITH WATER. IF IRRITATION DEVELOPS, DISCONTINUE USE AND CONTACT A PHYSICIAN. IF SWALLOWED, CONTACT A PHYSICIAN. DO NOT STORE ABOVE 40​0 ​C/110​0​F

Dosage & Administration

TEAR OPEN PACKET. UNFOLD TOWEL AND WIPE HANDS THOROUGHLY

Inactive Ingredient

WATER, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, ALOE BARBADENSIS EXTRACT, HYDROXYPROPYLCELLULOSE, ISOPROPYL ALCOHOL, PARFUM, PEG-7 GLYCERYL COCOATE, TETRAHYDROXYPROPYL ETHYLENEDIAMINE.

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