Otc - Active Ingredient
Alcohol 75%
Hand Sanitizer
FDA Label NDC 77257-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Huizhou Boymay Cosmetics Co. Ltd for the product Hand Sanitizer (NDC 77257-001). 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, otc - purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, otc - ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antiseptic
Use
For hand-washing to decrease bacteria on the skin, only when water is not available.
Warnings
Flammable, keep away from fire and flame. For external use only.
Otc - When Using
When using this product: Do not get into eyes. If contact occurs, rinse eyes thoroughtly with water. May discolor some fabrics.
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.
Otc - Ask Doctor
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Wet hand thoroughly with proudct and allow to dry without wiping.
Other Information
Store below 105 oF
Inactive Ingredient
Aqua(Water), Glycerin, Carbomer, Propylene Glycol, Sodium Hydroxide, Aloe Vera Leaf.
Otc - Questions
+1-315-636-0065
Package Label.Principal Display Panel
50ml NDC: 77257-001-11; 100ml NDC: 77257-001-12; 250ml NDC: 77257-001-13, 77257-001-14; 500ml NDC: 77257-001-15; 1000ml NDC: 77257-001-20
50ml And 100ml (Labels)
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