Antiseptic
FDA Label NDC 0363-7110

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Walgreen Co. for the product Antiseptic (NDC 0363-7110). 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 other, active ingredients, purpose, uses, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Other

Drug Facts

Active Ingredients

Benzalkonium Chloride 0.13%

Purpose

First Aid Antiseptic

Uses

  • Antiseptic cleansing of face, hands and body to decrease bacteria on skin without soap and water

Warnings

For external use only

Otc - Do Not Use

Do not use in the eyes. If this happens, rinse thoroughly with water.

Otc - Stop Use

Stop use and ask doctor if irritation or redness develop and persists for more than 72 hours

Otc - 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

  • tear open packet, unfold and use as a washcloth. Allow hands to dry without wiping.

Inactive Ingredients

Purified water, alcohol

Principal Display Panel – Packet Label

Well at
Walgreens

NDC 0363-7110-00

Antiseptic
Towelette

Benzalkonium Chloride/
First Aid Antiseptic


1 SINGLE-USE
PREMOISTENED TOWELETTE

Principal Display Panel – Packet Label (Wal03 0000 01)

Principal Display Panel – Packet Label (Wal03 0000 01)

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