Otc - Active Ingredient
Drug Facts
Active Ingredient:
Ethyl Alcohol 62 percent
Dawnmist Alcohol Gel Hand Sanitizer
FDA Label NDC 55504-3763
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Donovan Industries, Inc. for the product Dawnmist Alcohol Gel Hand Sanitizer (NDC 55504-3763). 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 otc - active ingredient, otc - purpose, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose: Antibacteria
Use: For handwashing to decrease bacteria on skin.
Warnings
Warnings:
Flammable. Keep away from heat or flame.
For external use only.
Do not use in the eyes.
In case of deep or puncture wounds, consult doctor.
In rare instances of irritation, discontinue use if irritation and redness develop.
If condition persists for more than 72 hours, consult a physician.
If swallowed, contact a physician or poison center.
Keep out of reach of children.
Dosage & Administration
Directions:
To decrease bacteria on skin, apply a small amount to palm.
Briskly rub covering hands with product until dry.
Inactive Ingredient
Inactive Ingredients: Water, Isopropyl Alcohol, Hydrogenated Starch, Carbomer, THP Ethylenediamine, and Fragrance.
Package Label.Principal Display Panel
DawnMist
Kills Germs Fast
Citrus Scent
Alcohol Gel
Hand
Sanitizer
2 FL. OZ. 59ml
Citrusalcoholgel59ml (Citrusscentupdate59ml)
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