Active Lngredient
Ethyl Alcohol
Solgreat Ethyl Alcohol
FDA Label NDC 73913-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Panatural Usa, Inc. for the product Solgreat Ethyl Alcohol (NDC 73913-006). 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 lngredient, purpose, uses, warnings, directions, other information, inactive ingredient, product labels, 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 help decrease bacteria on the skin, when water, soap & towel are not available.
• recommended for repeated use.
Warnings
For external use only.
Flammable. Keep away from fire or flame.
Do not apply around eyes. Do not use in ears & mouth.
When using this product, avoid contact with eyes. In case of contact flush eyes with water.
Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.
Keep out of reach of children.
Children must be supervised in use of this product.
Directions
• place enough product into your palms and thoroughly spread on both hands.
• rub into skin until dry.
Other Information
• store below 110℉ (43℃).
• may discolor certain fabrics or surfaces.
Inactive Ingredient
aloe barbadensis leaf juice, triethanolamine, glycerin, propylene glycol, tocopheryl acetate, water.
Product Labels
Image Description (Label 1)
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