Sanitizer
FDA Label NDC 68210-4118

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Spirit Pharmaceuticals Llc for the product Sanitizer (NDC 68210-4118). 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, active ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

• sanitizer to help reduce bacteria that potentially can cause disease
• recommend for repeated use

Warnings

For external use only. Flammable. Keep away from heat and flame.
Do not use • in children less than 2 months of age
• on open skin wounds
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When using this product
• keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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Stop use and ask a doctor if irritation or rash appears and lasts. These may be signs of a serious condition.

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

  • Spray directly to cover all surfaces. Rub together until dry
  • Children under 6 years of age should be supervised when using this product

Other Information

• Store between 15°-30°C (59°86°F)
• Avoid freezing and excessive heat above 40°C (104°F)
• may discolor certain fabrics or surfaces

Inactive Ingredients

 fragrance, glycerin, isopropyl myristate, water

Questions Or Comments?

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SANITIZER Spray

EFFECTIVELY KILLS 99.9% OF THE MOST COMMON GERMS/ BACTERIA

70%

ALCOHOL CONTENT

89 ml /148 ml 

* Please review the disclaimer below.