Active Ingredient
Ethyl Alcohol 75% v/v
Denatured Alcohol
FDA Label NDC 74047-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shantou Kangjie Daily Chemical Industry Co.,ltd for the product Denatured Alcohol (NDC 74047-003). 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, otc - purpose, indications & usage, warning, otc - do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antimicrobial
Indications & Usage
Hand Sanitizer to help reduce bacteria on skin.
Warning
Flammable liquid - Keep away from heat, spark, electrical, fire or flame.
Keep out of reach of children.
Otc - Do Not Use
Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.
Otc - When Using
When using this product,
Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask doctor if irrtation or rash appears and lasts.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Conter right away.
Otc - Stop Use
Stop use and ask doctor if irrtation or rash appears and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Conter right away.
Dosage & Administration
Place enough product in your palm to thoroughly spread on both hands.
Children under 6 years of age should be supervised when using this product.
Inactive Ingredient
Purified Water
Package Label.Principal Display Panel
003 (Label 20230605)
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