Freeman Packing Alcohol Wipe
FDA Label NDC 67772-018

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Jiangxi Sencen Hygienic Products Co., Ltd. for the product Freeman Packing Alcohol Wipe (NDC 67772-018). 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 - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, storage and handling, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active Ingredient

Chlorhexidine Gluconate........................1%

Alcohol....................................................40%

Otc - Purpose

Purpose:

Cleaning

Indications & Usage

Uses:

Clean and refresh hands and face without soap and water

Warnings

Warnings:

For external use on hands only. Store in a cool place. Stop use and ask for doctor if skin irritation developes

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Dosage & Administration

Directions:

Self dries in second. Leaves skin soft and smooth

Storage And Handling

Store in a cool place

Inactive Ingredient

Inactive Ingredient:

Isopropyl Alcohol, Benzalkonium Chloride, Glycerin, Aloe Vera Gel, Purified Water

Package Label.Principal Display Panel

Label (67772 016 01)

Label (67772 016 01)

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