Active Ingredient(S)
Ethyl Alcohol 70% v/v....Antimicrobial
Hand Sanitizer
FDA Label NDC 75705-005
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 Stelco Chemicals Co. Ltd for the product Hand Sanitizer (NDC 75705-005). 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 active ingredient(s), purpose, use, warnings, do not use, 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
Purpose
Antimicrobial, Hand Sanitizer
Use
Hand sanitizer to help reduce bacteria on the skin
Warnings
WARNING SFLAMMABLE. KEEP AWAY FROM FIRE OR FLAMEFOR EXTERNAL USE ONLY
Do Not Use
DO NOT USE this product in or near the eyes. In case ofeye contact, flush with plenty of water.
Otc - When Using
/
Otc - Stop Use
Stop use and consult a doctor if irritation or rash appears and lasts
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
Put enough product onto your palm and rub handstogether briskly until dry. Children under 6 years of ages hould be supervised when using this product.
Other Information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
Inactive Ingredients
Water(Aqua), Propylene Glycol, Glycerin, C10-30 AlkylAcrylate Crosspolymer, Triethanolamine, Vitamin E, Fragrance( Parfum)
Package Label - Principal Display Panel
1 (30ml)
2 (60ml)
3 (236ml)
4 (354ml)
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