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Ethyl Alcohol
FDA Label NDC 68345-652
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Pss World Medical, Inc. for the product Ethyl Alcohol (NDC 68345-652). 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 package label.principal display panel, indications & usage, inactive ingredient, warnings, otc - active ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Indications & Usage
DIRECTIONS: Place enough product in your palm to thoroughly cover your hands Rub hands together briskly until dryChildren under 6 years of age should be supervised when using this product.
Inactive Ingredient
Inactive ingredients Water (Aqua), Isopropyl Alcohol, Diisopropyl Sebacate, Glycerin, Isopropyl
Myristate, Propylene Glycol, Tocopheryl Acetate, Aminomethyl Propanol, Carbomer,
Fragrance (Parfum)
Warnings
WarningsFlammable. Keep away from fire or flame.For external use onlyWhen using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
Otc - Active Ingredient
Active Ingredient PurposeEthyl Alcohol 62% Antimicrobial
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