Aiwina Sanitizing Wet Wipes
FDA Label NDC 79011-001

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Hongkong Yifar Industrial Limited for the product Aiwina Sanitizing Wet Wipes (NDC 79011-001). 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 ingredients, purpose, uses, warnings, otc - keep out of reach of children, directions of use, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Benzalkonium Chloride 0. 10%

Alcohol 75%

Purpose

Antiseptic, Hand Sanitizer

Uses

  • For hand washing to decrease bacteria on the skin.
  • Recommended for repeat use.

Warnings

For external use only.
Keep out of reach of eyes. If contact occurs, rinse thoroughly with water.
Do not use if you are allergic to any of the ingredients.
Discontinue use if irritation or redness develops, and if condition persists for more than 72 hours consult a physician.

Otc - Keep Out Of Reach Of Children

• Keep out of reach of children unless under adult supervision.
• If swallowed, get medical help.

Directions Of Use

  • Wet hands thoroughly with product and allow to dry without rinse.
  • Children under six years of age should be supervised when using this product.

Other Information

Store in a dry place away from fire.

Inactive Ingredients

Water(Aqua), Glycerol, Propanediol, Aloe Vera Extract, Amino acid moisturizer, Hexadecylpyridinium Chloride, Vitamin E, Citric acid, Sodium citrate, Dodecyl polyglucoside.

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Label (Label)

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