Sanismart 2
FDA Label NDC 72130-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Registered Chemicals Corporation for the product Sanismart 2 (NDC 72130-002). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, inactive ingredient, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active ingredient

Benzalkonium Chloride 0.13%

Otc - Purpose

Purpose

Antimicrobial

Indications & Usage

Uses   •For hand washing to decrease bacteria on the skin

         •Recommended for repeated use

Warnings

Warnings

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes

thoroughly with water.

Stop use and ask a doctor if irritation or redness develop, or if condition 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.

Dosage & Administration

Directions   •Pump a small amount of foam into palm of hand.

•Rub thoroughly over all surfaces of both hands for 15 seconds.   •Rinse with potable water.

Inactive Ingredient

Inactive ingredients  Water (Aqua), coco-glucoside, laurtrimonium chloride,

coamidopropylamine oxide, citric acid

Package Label.Principal Display Panel

Image Description (Sani 21)

Image Description (Sani 21)

Image Description (Sani 22)

Image Description (Sani 22)

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