Techni-pro Foaming Hand Sanitizer
FDA Label NDC 59555-403

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by R & R Lotion, Inc for the product Techni-pro Foaming Hand Sanitizer (NDC 59555-403). 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, uses, 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 0.1%

Purpose

Antimicrobial

Uses

  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use

Warnings

For external use only

Otc - When Using

When using this product avoid contact with eyes. If contact with eyes, flush with water.

Otc - Stop Use

Stop use and ask a doctor if irritation or redness develops, or if condition persists 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

  • Pump a small amount of foam into palm of hand
  • Rub thoroughly over all surfaces of both hands
  • Rub hands together briskly until dry.

Inactive Ingredients

DI Water, Dihydroxypropyl PEG-5 Linoleammonium Chloride, Glycereth-2 Ocoate, Behentrimonium Chloride, Dihydroxyethyl Cocamine Oxide

Principal Display Panel - 3785 Ml Bottle Label

TECHNI-PRO

FOAMING
HAND SANITIZER

TestEquity Part #:
TNP-ICHS-GAL

PACKAGING SIZE: 128oz.

Principal Display Panel (3785 mL Bottle Label)

Principal Display Panel (3785 mL Bottle Label)

* Please review the disclaimer below.