Active Ingredient
Benzalkonium Chloride (0.13%)
Royal-plant Hand Sanitizer
FDA Label NDC 74606-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dor Properties Llc. for the product Royal-plant Hand Sanitizer (NDC 74606-100). 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, purpose, uses, warnings, keep out of reach of children, directions, inactive ingredient, royal-plant sanitizer, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Uses
Hand sanitizer for decreasing bacteria on skin
Warnings
For external use only
Do not use if you are allergic to any of the ingredients
When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. avoid contact with broken, irritated, or itching skin. Do not puncture or incinerate.
Stop use and ask a doctor if irritation or redness develops and condition persists for more than 72 hours
If pregnant or breast- feeding, ask a health professional before use.
Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Directions
Take appropriate amount onto your hand and spread it all the way to fingertips. Rub the contents until it dries.
Inactive Ingredient
Water, Ozone, Oxydants, Sodium Hypochlorite, Chlorine Dioxide, Sodium Chlorate
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