Hand Sanitizer With Aloe Vera
FDA Label NDC 60717-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Rna Pharma Llc for the product Hand Sanitizer With Aloe Vera (NDC 60717-001). 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, uses, flammable, keep away from fire and flames., for external use only, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Other

Drug Facts

Active Ingredient

ETHYL ALCOHOL 65%

Purpose

Antimicrobial

Uses

  • For hand sanitizer use to reduce bacteria on skin
  • Recommended for repeated use

Flammable, Keep Away From Fire And Flames.

For External Use Only

When Using This Product

  • do not get into eyes
  • if contact occurs, rinse eyes thoroughly with water

Stop Use And Ask A Doctor If

  • irritation and redness develops

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children

If swallowed, get medical help or contact a Poison Control Center right away

Directions

  • wet hands thoroughly with product and allow to dry without wiping

Inactive Ingredients

WATER, GLYCERIN, TETRAHYDROXYPROPYL ETHYLENEDIAMINE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER,

ALOE VERA GEL, FRAGRANCE

Principal Display Panel - 3785 Ml Bottle Label

NDC 60717-001-01

HAND SANITIZER with ALOE VERA

128 FL. OZ. (3785 mL)

Principal Display Panel (3785 mL Bottle Label)

Principal Display Panel (3785 mL Bottle Label)

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