Otc - Active Ingredient
CONTAINS:70% Ethyl Alcohol by volume
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Ethyl Rubbing Alcohol
FDA Label NDC 15231-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Comercializadora Jiquilpan S.a. De C.v. for the product Ethyl Rubbing Alcohol (NDC 15231-100). 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, dosage & administration, warnings, otc - keep out of reach of children, indications & usage, 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
INDICATIONS. To decrease germs in minor cuts and scrapes
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Dosage & Administration
DIRECTIONS. Apply to skin directly or with clean gauze cotton or swab For rubbing apply liberally and rub with hands.
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Warnings
WARNINGS.FOR EXTERNAL USE ONLY Will produce serious gastric disturbances if taken internally
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Otc - Keep Out Of Reach Of Children
KEEP OUT OF THE REACH OF CHILDREN. In case of accidental ingestion seek professional assistance or contact a Poison Control Center inmediately
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Indications & Usage
CAUTION Do not apply to irritated skin use in eyes or on mucous membranes incase of deep or puncture wounds consult a doctor
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Inactive Ingredient
INACTIVE INGREDIENTS .Denatonium Benzoate water
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Package Label.Principal Display Panel
Label (Label)
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