Active Ingredient
Ethyl Alcohol 70% V/V
Hand Sanitizer Spray
FDA Label NDC 87001-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Haian Kangrui Textile Co., Ltd. for the product Hand Sanitizer (NDC 87001-005). 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(s), warnings, do not use, when using this product，, stop use and ask a doctor, 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(S)
Hand sanitizer to help reducebacteria that potentially can causedisease. For use when soap and water arenot available.
Warnings
For external use only.Flammable. Keep away from fire and flame.
Do Not Use
·on children less than 2 months of age
·on open skin wounds
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 rashoccurs These.
may be signs of a seriouscondition.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Spray a small amount in your palm and briskly rub hands together until dry.
Supeivise children under 6 years of age when using this product to avoid swallowing.
Inactive Ingredients
Water，Propylene Glycol，Glycerin，Fragrance，Aloe Barbadensis Leaf Juice
87001-005-01
87001-005-01(1) (O 2)
87001-005-01(2) (P 3)
3 (Es 0)
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