Active Ingredient
Chlorhexidine Gluconate 0.5%
Antibacterial Protective Hand
FDA Label NDC 51811-658
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hanover Pen Corp Dba Hpc Global for the product Antibacterial Protective Hand (NDC 51811-658). 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, uses, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
Decrease bacteria on skin.
Recommended for repeated use.
Warnings
For external use only.
Flammable, keep away from fire or flame.
Otc - Do Not Use
Do not use in or near the eyes, in case of exposure rinse eyes throughly with water.
Do not use if you have preexisting rash condition.
Otc - Stop Use
Stop use and ask a doctor if irritation, redness or rash appear.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed get medical help or contact Poison Control Center right away.
Directions
Rub onto hands, as needed.
Inactive Ingredients
aloe barbadensis, aroma, carthamus tinctorius (safflower oleosomes), cellulose gum, cetyl alcohol, glycerin, glycerol stearate, panthenol, pvp, red 40 (ci 16035), tocopherol acetate, water, yellow 5 (CI 19140)
Package Label.Principal Display Panel
Drug Facts
Monarchhlpouch (Monarchhlpouch)
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