Active Ingredient
Alcohol 75%
Alcohol Wipes Patch
FDA Label NDC 77665-107
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Baihua Co., Ltd for the product Alcohol Wipes (NDC 77665-107). 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, do not use, when using, stop use, ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Use
Hand sanitizer to hel reduce bacteria on the skin
Warnings
Flammable, keep away from fire or flame, for external use only, don't use in or near the eyes, keep out of reach of children
Do Not Use
Do not use in or near the eyes
When Using
•for external use only, do not use in or near the eyes
Stop Use
• in case of contact, rinse yes thoroughly with water, stop use and consult with a physician if irritation develops and lasts for more than 72 hours
Ask Doctor
• in case of contact, rinse yes thoroughly with water, stop use and consult with a physician if irritation develops and lasts for more than 72 hours
Keep Out Of Reach Of Children
• keep out of reach of children, if swallowed, get medical help or contact a poison control center immediately
Directions
• storage: store at room temperature
• dispensing: open protective seal, pull out wipe, reseal
• use: wipe hands thoroughly For nail fungus,
• disposal: do not fulsh
Other Information
•If you are using other drugs, please consult your physician or pharmacist before using this product.
•Shielded from light, sealed, stored in a cool place (not more than 20°C).
Inactive Ingredients
purified water
Questions
Questions
Tel.400-055-8876
Principal Display Panel
1 (Pack)
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