Lonimax Hand Sanitising
FDA Label NDC 75556-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Shunan Industry&trade Co., Ltd for the product Lonimax Hand Sanitising (NDC 75556-001). 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 other, active ingredient(s), purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

NA

Active Ingredient(S)

Alcohol 75% 

Purpose

Antiseptic

Use

For hand washing to help decrease bacteria on the skin only when water is not available

Warnings

For external use only. Flammable. Keep away from fire and flame

Otc - When Using

When using this product do not get into eyes. When contact occurs, rinse eyes thoroughly with water

May discolor fabrics

Otc - Stop Use

Stop use and ask a doctor if irritation and redness develop

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.

Directions

  • Wet hands thoroughly with product and allow to dry without wiping

Other Information

  • Store below 105F

Inactive Ingredients

Water, Carbomer, Xanthan Gum, glycerin, Aloe Vera Extract, Allantoin, Vitamin E, Cellulose, Lactose, Jojoba Alcohol, Hyfrogenated

* Please review the disclaimer below.