Active Ingredient
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 50260-200
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Fercy Personal Care Products Co Limited for the product Hand Sanitizer (NDC 50260-200). 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, warning, directions, other information, 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
Purpose
Antiseptic
Uses
Hand sanitizer to reduce bacteria on the skin that potentially can cause disease
Warning
Flamable, keep away from children or flame.
For external use only.
Do not use in the eyes.In case of accidental contact with eyes,
flush eyes with water. Consult a doctor.
Discontinue use if irritation or redness develop.If condition
persists for more than 72 hours,consult a doctor.
Keep out of reach of children.If swallowed, get medical help
or contact a Poison Control Center right away.
Directions
Wet hands thoroughly with product and rub hands together until dry. No need to wash or rinse your hands
or use towels.
Supervise children under 6 years of age.
Other Information
·Do not store above 110 oF(43 oC).
·May discolor some fabrics, or may ham some wood finishes
and plastics.
Deionized water,Glycerin,Propylene Glycol,Triethanolamine,Carbomer,Methylparaben,Propylparaben,Fragrance.
Package Label.Principal Display Panel
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Phot Of Druglisting (Druglisting)
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