Antimicrobial Hand Wipe
FDA Label NDC 65460-3111

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Sas Safety for the product Antimicrobial Hand Wipe (NDC 65460-3111). 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, warnings, otc - do not use, otc - stop use, otc - 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

Ethyl Alcohol 66.5%

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 form fire or flame

Otc - Do Not Use

Do not use in the eyes. If this happens, rinse thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if irritation or redness develop and persist for more than 72 hours

Otc - Keep Out Of Reach Of Children

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 Ingredient

Inactive ingredients aloe vera, fragrance, purified water, triethanolamine

Package Label - Principal Display Panel – Pouch

FLU SHIELD ANTIMICROBIAL HAND WIPES

Kills 99.99% of germs

1 premoistened towelette

For Professional Use

Package Label (PRINCIPAL DISPLAY PANEL – POUCH)

Package Label (PRINCIPAL DISPLAY PANEL – POUCH)

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