Active Ingredient
Ethanol 77%
Skin Supply Hand Sanitizer
FDA Label NDC 76731-202
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bbhc Co., Ltd for the product Skin Supply Hand Sanitizer (NDC 76731-202). 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, directions, inactive ingredients, package label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
Hand sanitizer to help reduce bacteria on skin
Warnings
For external use on hands.
Flammable. Keep away from fire.
Do not use in or near the eyes. In case of contact, rinse with water.
Stop use and ask a doctor if irritation or rash appears and lasts.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.
Directions
Put product onto palm and then rub hands together.
Children under 6 years of age should be supervised when using this product.
Inactive Ingredients
Water, Glycerin, Ammonium Acryloyldimethyltaurate/VP Copolymer, Eucalyptus Globulus Leaf Oil, Aloe Barbadensis Leaf Juice, Chlorhexidine Digluconate, Sodium Chloride, Glucose
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