Smart Sense Vitamin E Sanitizer
FDA Label NDC 49738-482

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Kmart Corporation for the product Smart Sense Vitamin E Sanitizer (NDC 49738-482). 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 using this product and ask 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.

Active Ingredient

Ethyl Alcohol 70% (v/v)

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. If contact occurs, rinse thoroughly with water.

Stop Using This Product And Ask 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 (1-800-222-1222).

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)

Inactive Ingredients

Water (Aqua), Isopropyl Alcohol, Ethylhexylglycerin, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Propylene Glycol, Aminomethyl Propanol, Fragrance (Parfum).

Questions Or Comments?

1-800-842-7886

Label Copy

Image Of Label (20482l)

Image Of Label (20482l)

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