Otc - Active Ingredient
ethanol
Doctor Hand Fresh Gel
FDA Label NDC 70949-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by C-max Korea Co.,ltd. for the product Doctor Hand Fresh Gel (NDC 70949-002). 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, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, 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
Inactive Ingredient
water, carbopol, polysorbate 60, triethanolamine, peppermint oil
Otc - Purpose
Antiseptic
instant healthcare personnel hand antiseptic to reduce bacteria that potentially can cause disease
instant hand antiseptic to decrease bacteria on the skin
recommended for repeated use
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF THE CHILDREN
Indications & Usage
Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.
Supervise children in the use of this product.
Warnings
For external use only.
Flammable, keep away from fire or flame.
When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.
Stop use and ask a doctor if significant irritation or sensitization develops.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
for external use only
Package Label.Principal Display Panel
Label (Label)
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