Active Ingredient(S)
Alcohol 70% v/v. Purpose: Antiseptic
Hand Sanitizer
FDA Label NDC 75586-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dongyang Mukang Pharmaceutical Factory for the product Hand Sanitizer (NDC 75586-010). 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(s), purpose, use, warnings, 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
Purpose
Antiseptic, Hand Sanitizer
Use
Hand Sanitizer to help reduce bacteria on the skin that could cause disease.
Recommended for repeated use.
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
Otc - When Using
When using this product do not use in or near the eyes. In case of contact , rinse eyes thoroughly with water.
- Avoid contact with broken skin
- Do not inhale or ingest.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash oppears and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Place enough product in your palm to thoroughly cover your hands
- Rub hands together briskly until dry
- Children under 6 years of ages should be supervised when using this product.
Other Information
- Do not store above 110℉（40℃）
- May discolor certain fabrics or surfaces
Inactive Ingredients
Water, Carbomer, AMP-95 aminomethly propanol, jasmine scent, aloe vera, FD&C yellow no.5(tartrazine), and FD&C blue no.1
Package Label - Principal Display Panel
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