Hand Sanitizer Liquid
FDA Label NDC 52854-600

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Tropical Seas, Inc. for the product Hand Sanitizer (NDC 52854-600). 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 ingredients, purpose, uses, warnings, otc - do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Drug Facts

→ Active Ingredients

→ Purpose

→ Uses

→ Warnings

→ Otc - Do Not Use

→ Otc - When Using

→ Otc - Stop Use

→ Otc - Keep Out Of Reach Of Children

→ Directions

→ Inactive Ingredients

→ Other Information

→ Questions Or Comments?

→ Principal Display Panel - Bottle Label

Drug Facts

Active Ingredients

Ethyl Alcohol 64.325%

Purpose

Antiseptic

Uses

for sanitizing hands to help reduce bacteria on the skin.
for deodorizing hands to help reduce odors on the skin.

Warnings

For external use only

Otc - Do Not Use

Do not use on damaged or broken skin

Otc - When Using

When using this product keep out of eyes. Rinse with water to remove.

Otc - Stop Use

Stop use and ask a doctor if rash occurs

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

rinse solids & slime from hands if possible.
pat dry.
put a thumbnail size amount in your palm and rub hands together briskly until dry.
repeat as needed.
children under 6 months: As a doctor