Wancare
FDA Label NDC 81314-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kaf Grup Saglik Hizmetleri Insaat Sanayi Ve Ticaret Limited Sirketi for the product Wancare (NDC 81314-101). 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(s), purpose, use(s), 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(S)
Ethyl Alcohol 70% (v/v)
Purpose
Antiseptic
Use(S)
Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.
Warnings
For external use only.
Flammable. Keep away from fire 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, rinse eyes thoroughly with water. Do not inhale or ingest.
Stop use and ask a doctor if irritation or rash appears and lasts. Condition persists for more than 72 hours.
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.
Directions
Place enough product in your palm to thoroughly cover your hands.
Rub hands together briskly until dry.
Children under 6 years of age should be supervised when using this product.
Other Information
Store between 5-40C (41-104F)
Avoid freezing and excessive heat above 40C (104F)
Inactive Ingredients
Water (Aqua), Glycerin, Fragrance
Packaging
Image (81314 101 2)
Image (81314 101 4)
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