Puroma Hand Sanitizer Wipe Alcohol Free
FDA Label NDC 80948-011

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zenith Micro Control for the product Puroma Hand Sanitizer Wipe Alcohol Free (NDC 80948-011). 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 drug facts, active ingredient, purpose, uses, warnings, keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Benzalkonium chloride 0.13%

Purpose

Antibacterial

Uses

Hand Sanitizer to help reduce bacteria on skin.

Warnings

• For external use only.
• When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
• Stop use and ask a doctor if irritation or rash appears and lasts.

Keep Out Of Reach Of Children

except under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Pull out one sheet from the pack. Clean hands or affected area.

Discard wipes in trash receptacle after use.

Do not flush.

Close lid after each used to keep wipes fresh.

Inactive Ingredients

Aqua, Coco Glucoside, Caprylyl Glycol, Cetrimonium Chloride, Behetrimonium Chloride, Decyl Glucoside, Peg-7 Glyceril Cocoate, Glyceril Oleate, Glycerin, Phenoxyethanol, Methylisothiozolinone, Methylchloro Isothiozolinone, Betain, Aloevera Leaf, Polysorbate 20 , Propylene glycol.

Other Information

• Store below 104°F (40°C)

* Please review the disclaimer below.