Olife Wet Wipe For Hands
FDA Label NDC 80908-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Natural O'life, S.a. De C.v. for the product Olife Wet Wipe For Hands (NDC 80908-000). 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, do not use, stop use and ask a doctor, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Ethyl Alcohol 75%

Purpose

Antiseptic.

Uses

  • For handwashing to decrease bacteria on skin when soap and water is not available.

Warnings

For external use only.

Flammable: keep away from fire or flame.

Do Not Use

in the eyes. If this happens, rinse thoroughly with water.

Stop Use And Ask A Doctor

if irritation or redness develop and persist for more than 72 hours.

Keep Out Of Reach Of Children

if swallowed get medical help or contact a Poison Control Center right away.

Directions

  • Tear open packet, remove towelette.
  • Wipe hand/wrist areas for 15 seconds and discard
  • supervise children under 6 years of age.

Inactive Ingredients:

Water, Vegetable glycerine, Propylene glycol.

Package Labeling:

Bottle (Bottle)

Bottle (Bottle)

* Please review the disclaimer below.