Active Ingredient
Ethyl Alcohol 70%
Hand Sanitizer
FDA Label NDC 75230-002
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 Hongshiliang Health Technology Co., Ltd. for the product Hand Sanitizer (NDC 75230-002). 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, purpose, use, warnings, keep out of reach of children, directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
Use To decrease bacteria on the skin
Warnings
Flammable. Keep away from fire or flame.
For external use only
When using this product do not use in or near the
eyes. In case of contact, rinse eyes thoroughly with
water. Stop use and ask a doctor if irritation or
rash appears and lasts.
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
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 above 110°F(43°C)
●may discolor some fabrics
●harmful to wood finishes and plastics
Inactive Ingredients
Water, ,Glycerin,Carbomer,Triethanolamine
* Please review the disclaimer below.
