New Sanicol Advanced Antibacterial Hand Sanitizer
FDA Label NDC 79254-019

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Am Beauty Distributors Inc. for the product New Sanicol Advanced Antibacterial Hand Sanitizer (NDC 79254-019). 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, use, warnings, when using this product, stop use and ask a doctor if, 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 75%

Purpose

Antibacterial 

Use

  • Hand sanitizer to help reduce bacteria on the skin

Warnings

For external use only: hands

Flammable, keep away from fire or flame.

When Using This Product

  • keep out of eyes, in case of contact with eyes, flush thoroughly with water
  • avoid contact with broken skin
  • do not inhale or ingest

Stop Use And Ask A Doctor If

  • irritation or rash develops 
  • condition persists for more than 72 hours

Keep Out Of Reach Of Children

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

Directions

  • Put enough product in palm to cover hands and rub hands together briskly until dry.
  • Children under 6 years of age should be supervised when using SANICOL®

Other Information

  • Store below 110F (43C)
  • May discolor certain fabrics or surfaces

Inactive Ingredients:

Water (Aqua), Aloe Barbadensis Leaf Extract, Acrylates/C10-30 alkyl Acrylate Crosspolymer, Tetrahydroxypropyl Ethylenediamine

Package Labeling:

Label (Label)

Label (Label)

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