Wancare
FDA Label NDC 81314-302

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 81314-302). 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

→ Drug Facts

→ Active Ingredient(s)

→ Purpose

→ Use(s)

→ Warnings

→ Otc - Keep Out Of Reach Of Children

→ Directions

→ Other Information

→ Inactive Ingredients

→ Packaging

Drug Facts

Active Ingredient(S)

Ethyl Alcohol 75% v/v

Purpose

Antiseptic

Use(S)

• Hand Sanitizer wet wipes to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

• Recommended for repeated use.

Warnings

For external use only.

Flammable. Keep away from heat, fire, sparks or flame.

Do not use

• in children less than 2 months of age
• on open skin wounds

When using if swallowed, rinse mouth with plenty of water.

Get medical advice, If in eyes, remove contact lenses immediately. Rinse your eyes with plenty of clean water. Get medical attention if symptoms persist.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.