Bluzen Hand Sanitizer Wintermint
FDA Label NDC 79200-607
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Remcoda, Llc for the product Bluzen Hand Sanitizer Wintermint (NDC 79200-607). 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, purpose, indications & usage, 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
Ethyl alcohol 70% v/v
Purpose
Antiseptic
Indications & Usage
Uses ■ hand sanitizer to help reduce bacteria on skin
Warnings
Flammable, keep away from fire/flame
For external use only
When using this product ■ do not get into eyes. In case of contact, rinse eyes thoroughly with water
■ do not inhale or ingest
Stop use and ask a doctor if irritation and redness develop
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
■ wet hands thoroughly with product and allow to dry without wiping
■ supervise children under 6 years of age when using this product to avoid swallowing
Other Information
■ Store below 104°F (40°C)
Inactive Ingredients
water, aloe barbadensis leaf juice, glycerin, fragrance
Otc - Questions
Questions? 1-800-777-1603
Packaging
Image (7920060702)
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