Active Ingredient(S)
75% Alcohol(V/V).
Pro-tex Hand Sanitizer
FDA Label NDC 52728-020
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 Enchant Cosmetic Co., Ltd. for the product Pro-tex Hand Sanitizer (NDC 52728-020). 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, otc - keep out of reach of children, dosage & administration, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial and dialy hand cleaning.
Have antibacterial effect to staphylococcus aureus, escherichia coli, candida albicans.
Use
Squeeze out a small amount of formula properly and knead it with both hands.
Lasting for 1-3 minutes.
Warnings
Do not take the external product orally;
Do not touch the wound;
Do not contact the child directly;
If you contact the eyes carelessly, wash them with water in time;
Do not use this product instead of drugs;
Do not use it if you are allergic to alcohol.
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.
Dosage & Administration
Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
Keep away from sunlight and store in a cool and dry place.
Inactive Ingredients
Water(Aqua), Carbomer, Aminomethyl propanol, Aloe Barbadensis Leaf Juice, Sodium Hyaluronate.
Package Label - Principal Display Panel
237 mL in 1 BOTTLE NDC: 52728-020-01
237ml Label (237label)
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