Otc - Active Ingredient
Ethyl Alcohol 75.0%
Hand Sanitizer
FDA Label NDC 75468-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Henan Deyuanxiang Biological Technology Co., Ltd. for the product Hand Sanitizer (NDC 75468-001). 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 otc - active ingredient, purpose, use, warnings, otc - keep out of reach of children, directions, inactive ingredients, other, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
●to decrease bacteria on the skin that could
cause disease ● recommended for repeated use
Warnings
For external use only: hands.
Flammable. Keep away from fire or flame.
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
Stop use and ask a doctor if●iritation and redness
develops●condition persists for more than 72 hours
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
rub into skin until dry●for children under 6, use only
under adult supervision●not recommended for infants.
Inactive Ingredients
Water, Carbomer,Triethanolamine.
Other
Other information
●Do not store above 105°F ●May discolor some
fabrics●Harmful to wood finishes and plastics
* Please review the disclaimer below.
