Indications & Usage
for hand washing to decrease bacteria on the skin only when water is not available.
Ultra Defense Sani Smart Hand Sanitizer
FDA Label NDC 51522-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Gold Orient International Limited for the product Ultra Defense Sani Smart Hand Sanitizer (NDC 51522-001). 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 indications & usage, drug facts active ingredients, purpose, dosage & administration, inactive ingredients:, warning, otc - keep out of reach of children, otc - when using, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Drug Facts Active Ingredients
Ethyl Alcohol 65%
Purpose
Antiseptic
Dosage & Administration
- wet hands thoroughly with product and allow to dry without wiping
Inactive Ingredients:
Water(Aqua), Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Polysorbate 20, Sodium Hydroxide
Warning
- For External Use Only.
- Flammable, keep away from fire and flames
Otc - Keep Out Of Reach Of Children
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.
Otc - When Using
When using this product
- do not get into eyes.
- if contact occurs, rinse eyes thoroughly with water
Otc - Stop Use
Stop us and ask a doctor if
- irritation and redness develop
* Please review the disclaimer below.
