Active Ingredient(S)
Ethyl Alcohol 94%
Zapro Hand Sanitizer
FDA Label NDC 75209-011
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 Zapro Hand Sanitizer (NDC 75209-011). 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, when using this product, 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
Use
for hand washing to decrease bacteria on he skin， only when water is not ava able
Warnings
Flammable—Keep away from fire and flames
For external use only
Do Not Use
Do not get into eyes
lf contact occurs， rinse thoroughly with water
When Using This Product
When using this product
Do not get into eyes
lf contact occurs， rinse thoroughly with water
Stop use and ask a doctor if
Irritation and redness develop
Keep out of reach of children.If swallowed， get medical help or contact a Poison Control Center right away.
Otc - Stop Use
Stop use and ask a doctor if
Irritation and redness develop
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
Press pump twice to dever two s quits of product on to the pam of your hand
Rub hands together and allow to dry without wiping
Other Information
May discolor fabrics or surfaces
Store below 110°F(43°C)
Inactive Ingredients
water, cellulosico-polymer, zinc pyrithione
Package Label - Principal Display Panel
75209-011-01 250ml
75209-011-02 2000ml
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