Onid Wipe Swab
FDA Label NDC 71441-180

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Onid Technology Corp for the product Onid Wipe (NDC 71441-180). 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 ingredient, purpose, uses, directions, keep out of reach of children, inactive ingredients, principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 75%

Purpose

Antiseptic

Uses

  • For hand washing to decrease bacteria on the skin
  • Reccomended for repeated use

Directions

  • open packet
  • remove and unfold wipe
  • wipe hands throughly for approximately 15 seconds
  • do not flush

Keep Out Of Reach Of Children

If swollowed get medical help or contact Poision Control Center imediately.

Inactive Ingredients

Taiwan Hinoki oil, titanium dioxide, water

* Please review the disclaimer below.