Nsi Sanitizing Wipes Patch
FDA Label NDC 82716-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Northern Safety Co., Inc. for the product Nsi Sanitizing Wipes (NDC 82716-000). 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 ingredient [s], purpose, use [s], warnings, do not use, stop use and ask a doctor if, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient [S]

75% Ethyl Alcohol

Purpose

Antiseptic

Use [S]

  • Helps reduce bacteria on the skin
  • Recommended for repeated use

Warnings

For external use only

Flammable, keep away from fire or flame

Do Not Use

in eyes. If contact occurs, flush thoroughly with water.

Stop Use And Ask A Doctor If

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

Keep Out Of Reach Of Children

If swallowed, get medical help or contact the Poison Control center right away.

Directions

  • Use on wipe per object to avoid cross contamination
  • Allow to dry without wiping
  • Discard wipe in trash receptacle after use
  • Do not flush
  • For dispensing, peel back front label at tab
  • Remove towelettes as needed
  • Reseal pouch by pressing label firmly back into place

Other Information

  • Store below 104 °F (40 °C)
  • May discolor certain fabrics.

Inactive Ingredients

Glycerin, Water.

Package Labeling:

Label (Label)

Label (Label)

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