Active Ingredient(S)
Ethyl Alcohol 62% v/v. Purpose: Antiseptic
Instant Hand Sanitizer
FDA Label NDC 75236-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Pujiang Shijiali Cosmetics Co., Ltd. for the product Instant Hand Sanitizer (NDC 75236-001). 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 active ingredient(s), purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
To reduce bacteria on the skin that could cause disease
Recommended for repeated use
Use anywhere without water
Warnings
For external use only -hands
Flammable. Keep away from heat and flame
Otc - When Using
When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water.
Avoid contact with broken skin
Do not inhale or ingest
Otc - Stop Use
Discontinue if skin becomes irritated and ask a doctor
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. In case of accidental ingest, seek professional assistance or contact a Poison Control Center right away.
Directions
- Wet hands thoroughly with product and rub until dry without wiping
- For children under 6, use only under adult supervision
- Not recommended for infants
Other Information
Do not store above 105F
May discolor some fabrics
Harmful to wood finishes and plastics
Inactive Ingredients
Water, propylene glycol, glycerin, carbomer, triethanolamine, fragrance
Package Label.Principal Display Panel
Image Description (Shijiali)
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