Phoenix Hand Sanitizer Gel
FDA Label NDC 80666-555
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Thanh Cong Pharmaceutical And Trading Co.,ltd for the product Phoenix Hand Sanitizer Gel (NDC 80666-555). 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 drug facts, active ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethanol 70% + 3%
Purpose
Antiseptic
Uses
• Help to clean hand quickly.
• Resist bacteria without water, deodorizer.
Warnings
Warnings: For external use only. Flammable. Keep away from heat or flame.
Do not use
• In children less than 2 months of age.
• On open skin wounds.
When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
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 at 1 - 800 -222 - 1222.
Directions
• Use about 5 ml of solution, massage lightly whole hand that need to be cleaned until dry.
• Do not need to wash again with water.
Other Information
• Store between 15-30°C (59-86°F).
• Avoid freezing and excessive heat above 40°C (104°F).
Inactive Ingredient
Inactive ingredients: Carbomer, Triethanolamine (TEA), Water.
Packaging
Phoenix1 (80666555 1)
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