Armour
FDA Label NDC 78087-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sozal Kimya Sanayi Ve Ticaret Anonim Sirketi for the product Armour (NDC 78087-001). 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 drug facts, active ingredient[s], purpose, uses[s], warnings, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient[S]
Ethyl Alcohol 80% w/w
Purpose
Antiseptic
Uses[S]
▪ Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For external use only.
Flammable: Keep away from heat or flame.
Do not use
▪ In children less than 2 months of age
▪ On open skin wounds
When using this product ▪ keep out of eyes, ears, and mouth, in case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.
Directions
• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
Store between 15-30°C (59-86F) Avoid freezing and excessive heat above 40°C (104F)
Inactive Ingredients
Deionized water, glycerine, hydrogen peroxide
Other
Alcohol-Based
MANUFACTURED BY
SOZAL
SOZAL KIMYA SAN. ve TIC. A. S.
KOSAB Guvenli Sok.
No. 7 Bursa/ TURKEY
Packaging
Untitled (Label1)
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