Careone
FDA Label NDC 41520-410

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 (NDC 41520-410). 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.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 65%

Purpose

Antiseptic

Uses

  • to decrease 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 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.

Directions

  • apply a small amount to your palm and rub hands together briskly until dry.
  • children under 6 years old should be supervised when using this product.

Other Information

  • store at a room temperature below 110°F (43°C)

Inactive Ingredients

Water (Aqua), Fragrance (Parfum), Carbomer, Aminomethyl Propanol, Tocopheryl Acetate, Isopropyl Alcohol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Glycerin, Mannitol, Cellulose, Hydroxypropyl Methylcellulose, Iron Oxides (CI 77491), Red 33 (CI 17200), Red 40 (CI 16035), Yellow 5 (CI 19140).

Label Copy

Image Of The Label (19383l)

Image Of The Label (19383l)

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