O Well Sanitizing Hand Wipes Cloth
FDA Label NDC 77133-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Alcove Brands for the product O Well Sanitizing Hand Wipes (NDC 77133-002). 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, directions, warnings:, do not use, when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Alcohol 75%

Purpose

Disinfection

Uses

  • Hand Sanitizer to help reduce bacteria on the skin

Directions

  • Open the flip and tear the seal sticker
  • Remove the wipes from the middle hole and use
  • Close the flip to prevent the wipes from drying out

Warnings:

For external use only.

Do Not Use

  • in or contact the eyes.

When Using This Product

  • These wipe do not replace wipe used for medical procedures. These wipes are meant for general cleansing.
  • Keep in a dry place away from fire.
  • Discontinue use if irritation and redness develop. If the condition persists for more than 72 hours, consult a physician.
  • Please close the lid after dispending to maintain purity. Alcohol by nature evaporates quickly.
  • Store below 95°F (35°C).

Keep This Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Inactive Ingredients

Aqua, Glycerin, Benzalkonium

Package Labeling:20 Count

Label (Label)

Label (Label)

Package Labeling:50 Count

Label2 (Label2)

Label2 (Label2)

Package Labeling:50 Individual Packets

Label3 (Label3)

Label3 (Label3)

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