Antiseptic Wipe
FDA Label NDC 64709-105

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Diamond Wipes International for the product Antiseptic Wipe (NDC 64709-105). 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, inactive ingredients, label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Active Ingredient

→ Purpose

→ Uses

→ Warnings

→ Keep Out Of Reach Of Children

→ Directions

→ Inactive Ingredients

→ Label

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses

• for hand sanitizing to decrease bacteria on skin when water and soap are not available

• safe for repeated

Warnings

For external use only

When using this product do not use in or near eyes. If contact occurs, flush thoroughly with water

Discontinue use if irritation or redness develops if condition persists for more than 72 hours contact a doctor

Keep Out Of Reach Of Children

Keep out of reach of children unless under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away

Directions

• tear open packet, remove wipe

• wet hands thoroughly with product

Inactive Ingredients

Water, Aloe Barbadensis Leaf Juice, Citric Acid, Fragrance, Glycerin, Hamamelis, Virginiana (Witch Hazel) Bark/Leaf/Twig Extract, Phenoxyethanol, Polysorbate 20, Tocopheryl Acetate