Careone Vitamin E Hand Sanitizer
FDA Label NDC 41520-059

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by American Sales Company for the product Careone Vitamin E Hand Sanitizer (NDC 41520-059). 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, uses, 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 65%

Purpose

Antiseptic

Uses

to help reduce bacteria on the skin.

Warnings

For external use only.

  • flammable.
  • keep away from source of heat or fire.

When Using This Product

avoid contact with eyes. In case of contact, rinse thoroughly with water.

Stop Use And Ask A Doctor If

irritation or redness develops and lasts.

Keep Out Of Reach Of Children.

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

  • put enough product in your palm to cover hands and rub hands together until dry.
  • children under 6 years should be supervised when using this product.

Other Information

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

Inactive Ingredients

Water (Aqua), Isopropyl Alcohol, Aloe Barbadensis Leaf Juice, Glycerin, Isopropyl Myristate, Carbomer, Tocopheryl Acetate, Aminomethyl Propanol, Fragrance (Parfum).

Questions Or Comments?

1-877-846-9949

Label Copy

Image Of The Label (22508l)

Image Of The Label (22508l)

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