Antibacterial Hand Sanitizer With Vitamine E
FDA Label NDC 61180-111

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cj Pharmaceuticals, Llc for the product Antibacterial Hand Sanitizer With Vitamine E (NDC 61180-111). 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 drug facts, purpose, use, warnings, otc - when using, otc - stop use, otc - 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

Drug Facts

Active Ingredients

Ethyl Alcohol 70%

Purpose

Antiseptic

Use

as hand sanitizer to help reduce bacteria on the skin

Warnings

Flammable. Keep away from fire or flame.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 with water.

Otc - Stop Use

Stop use and ask a doctor if irritation or redness develops.

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

  • apply palmful to hands
  • rub hands together vigorously until dry
  • supervise children in the use of this product

Other Information

  • store below 110°F (43°C)
  • may discolor certain fabrics or surfaces.

Inactive Ingredients

Water, Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propanol, Fragrance, Propylene Glycol, Isopropyl Myristate, Aloe barbadensis Leaf Juice (Aloe Vera), Tocopheryl Acetate (Vitamin E).

Package Label

ANTIBACTERIAL
HAND
SANITIZER with
VITAMIN E
Compare to Purell®
8 FL OZ (236 mL)

Label (Image 01)

Label (Image 01)

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