Active Ingredient(S)
Alcohol62%
Hand Sanitizer
FDA Label NDC 75209-009
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Mingliu Technology Dail-use Chemical Co., Ltd. for the product Hand Sanitizer (NDC 75209-009). 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
Antiseptic
Use
For Hand Sanitizing
Warnings
For external use only-hands.
Flammable. Keep away from heat and flame.
Do Not Use
/
Otc - When Using
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
Stop use and ask a doctor if skin irritation develops.
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 For children under 6 use only under adult Supervision. Not recommended for infants.
Other Information
Do not store above105°F.
May discolor some fabrics.
Harmful to wood finishes and plastics.
Inactive Ingredients
Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water
Package Label - Principal Display Panel
53 (53ml)
60 (60ml)
* Please review the disclaimer below.
