Foaming Hand Sanitizer
FDA Label NDC 79724-375

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Specialty Water Resources, Llc for the product Foaming Hand Sanitizer (NDC 79724-375). 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, directions, inactive ingredients, packaging, 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

Antimicrobial

Uses

• For hand sanitizing to decrease bacteria on the skin
• Recommended for repeated use

Warnings

For external use only
When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Directions

• Pump a small amount of foam into palm of hand
• Rub thoroughly over all surfaces of both hands
• Rub hands together briskly until dry

Inactive Ingredients

Water, d-glucopyranose, oligomeric, decyl octyl glycosides, glycerol, methylisothiazolinone, and citric acid.

Packaging

Image (79724375 81)

Image (79724375 81)

Image (79724375 81(df))

Image (79724375 81(df))

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