Wet Wipes
FDA Label NDC 20276-433

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Delta Brands, Inc for the product Wet Wipes (NDC 20276-433). 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, do not use, when using this product, stop use, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Benzethonium Chloride 0.3%

Purpose

Antibacterial

Uses

Decreases bacteria on the skin

Warnings

For external use only

Do Not Use

Over large areas of the body if you are allergic to any of the ingredients

When Using This Product

When using this product do not get into eyes.If contact occurs, rinse thoroughly with water.

Stop Use

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours

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

For adults and children 2 years and over use on hands and face to clean and refresh, allow skin to air dry.  For children under 2 years of age ask a doctor before use.

Inactive Ingredients

Water, Propylene Glycol, Cocamidopropyl Betaine, PEG-7 Glyceryl Cocoate, Fragrance, Benzyl Alcohol, Methylchloroisothiazolinine, Methylisothiazolinone, Tetrasodium EDTA, PEG-40 Hydrogenated Castor Oil, Cetrimonium Chloride, Citric Acid, Aloe Vera Extract, Alphatocopherol Acetate (Vitamin E)

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Package Label

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