Clorox Care Concepts Hand Sanitizer
FDA Label NDC 26509-0002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by The Clorox Company for the product Clorox Care Concepts Hand Sanitizer (NDC 26509-0002). 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, directions, inactive ingredients, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Dimethicone 1.25 percent

Alcohol 67 percent

Purpose

Skin Protectant

Antiseptic

Use

  • Helps prevent and temporarily protect dry, cracked, chafed skin.

    • Hand sanitizer to decrease bacteria on the skin that potentially can cause disease

Warnings

For external use only

Flammable. Keep away from fire or flame.
For external use only.

Directions

  • Apply liberally as often as needed.

    • Wet hands thoroughly with product and allow to dry without wiping.

Inactive Ingredients

Water, Mineral Oil, Propylene Glycol, Glyceryl Distearate, Glyceryl Stearate, Microcrystalline Wax, Cetyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Polysorbate 20, Simmondsia Chinensis (Jojoba) Seed Oil, Tetrahydroxypropyl Ethylenediamine, Phenoyethanol, Fragrance, Methylparaben, Benzatriazoyl Dodecyl p-Cresol, Ethylparaben, Butylparaben, Propylparaben, Isobutylparaben

Water, Isopropyl Alcohol, Glycerin, Glyceryl Laurate.

Other Information

Store in a cool, dry place below 104 deg F (40 deg C).

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