Dawnmist Alcohol Hand Sanitizer
FDA Label NDC 65517-1007

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dukal Llc for the product Dawnmist Alcohol Hand Sanitizer (NDC 65517-1007). 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, keep out of reach of children., directions:, inactive ingredients:, package label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antibacterial Agent

Use:

For hand washing to decrease bacteria on skin.

Warnings

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

Do not use in the eyes ■ In rare instances of irritation,
discontinue use if irritation and redness develop ■ If
condition persists for more than 72 hours, consult a
physician

Keep Out Of Reach Of Children.

■ If swallowed, contact a physician or poison center ■ Use only as directed

Directions:

To decrease bacteria on skin, apply a small amount to palm. Briskly rub covering hands with product until dry.

Inactive Ingredients:

Water, Glycerin, Propylene Glycol, DMDM Hydantoin, Aminomethyl Propanediol, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Vera Leaf Extract, Tocopherol

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