Heys Hand Sanitizer
FDA Label NDC 77404-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Heys America Ltd. for the product Heys Hand Sanitizer (NDC 77404-001). 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 heys hand sanitizer, heys hand sanitzer, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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Heys Hand Sanitizer

Ethyl Alcohol 70% v/v

Antimicrobial

Use: Hand Sanitizer to help reduce bacteria on the skin.

Warnings: For external use only

Flammable: Keep away from heat and flame.

Stop use and ask a a doctor if irritation or redness develops.

Keep out of reah of children. If swallowed, get medical help or contact a Poison Control Center.

Directions: wet hands thoroughly with product and rub into skin until dry. children under 6 years of age should be supervised by an adult when using.

Store at 20 C to 25 C (68 to 77 F)

May discolor certain fabrics

Water

Carbomer 940

Fragrance

Glycerin

Polypropylene glycol

Triethanolamine

Aloe Barbadensis Leaf Juice

D-alpha Tocopheryl acetate

236 mL Label (Heys Hand Sanitizer Heys Pkg Us V5)

236 mL Label (Heys Hand Sanitizer Heys Pkg Us V5)

236 mL NDC: 77404-001-08

Heys Hand Sanitzer

When using this product avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

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