Otc - Active Ingredient
Active ingredients
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 47993-232
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Jiangbei Ocean Star Trading Co.,ltd for the product Hand Sanitizer (NDC 47993-232). 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, warnings, otc - do not use, otc - when using, otc - ask doctor, otc - keep out of reach of children, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antiseptic
Warnings
Warnings: For external use only. Flammable. Keep away from fire or flame.
Otc - Do Not Use
Do not apply around eyes. Do not use in ears & mouth.
Otc - When Using
When using this product，avoid contact with eyes. In case of contact flush eyes with water.
Otc - Ask Doctor
Stop use and as a doctor if redness or irritation develop and persist for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children， Children must be supervised in use of this product.
Indications & Usage
Uses：
Hand sanitizer to help decrease bacteria on the skin.
When water, soap & towel are not available.
Recommended for repeated use.
Dosage & Administration
Directions:
Pump as needed into your palms and thoroughly spread on both hands.
Rub into skin until dry.
Other Safety Information
Store at 20 ℃（68 to77℉）
May discolor fabrics.
Inactive Ingredient
Inactive Ingredients:
Water,Carbomer 940,Triethanolamine,Glycerin,Aloe barbadensis leaf juice,Fragrance,CI19140,CI42090
Package Label.Principal Display Panel
237 (237ml)
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