Hand Sanitizer
FDA Label NDC 71120-113

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Sanit Technologies Llc for the product Hand Sanitizer (NDC 71120-113). 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, warnings, uses, directions, keep out of reach of children., inactive ingredients:, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Warnings

  • For external use only.
  • ­­­­Keep out of eyes. In case of contact, flush eyes with water.
  • Stop use and consult a doctor if irritation or redness develops.

Uses

• To decrease bacteria on the skin.

Directions

•Rub thoroughly over all surfaces of both hands.
•Rub hands together briskly until dry.

Keep Out Of Reach Of Children.

  • If swallowed, get medical help or contact a Poison Control Center immediately.

Inactive Ingredients:

water, cetrimonium chloride, laurtrimonium chloride, dihydroxyethyl cocamine oxide, glycereth-17 cocoate, propylene glycol, diazolidinyl urea, methyl paraben, propyl paraben, citric acid, dihydroxypropyl PEG-5 linoleammonium chloride.

Product Label

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