Touchpoint Wipes Cloth
FDA Label NDC 70924-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Innocore Sales & Marketing Inc for the product Touchpoint Wipes (NDC 70924-001). 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 other, active ingredient, purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13 %

Purpose

Antimicrobal

Use

Hand sanitizer to help reduce bacteria on the skin.

Recommended for repeated use.

Warnings

For external use only.

Otc - When Using

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly in water.

Otc - Stop Use

Discontinue use if irritation and redness develop. If conditions persist for more than 72 hours, consult a physician.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Directions

  • Wet hands thoroughly with product and allow to dry.
  • Children under 6 years of age should be supervised when using this product.
  • Be sure to use entire wipe.
  • Discard after single use.

Inactive Ingredients

Water, propylene glycol, decyl/lauryl glucoside, glucoside, perfume, phenoxyethanol, benzoic acid, dehydroacetic acid.

Principal Display Panel - 2 Roll Case Label

Touchpoint
wipes

Kills 99.99%
of most common germs
that may cause illness

Sanitizing
wipes

1500
count

Premium fabric quickly
removes dirt and soil

Principal Display Panel (2 Roll Case Label)

Principal Display Panel (2 Roll Case Label)

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