Active Ingredient
Benzalkonium Chloride 0.13%
Xtra Spray
FDA Label NDC 51628-4439
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by My Imports Usa Llc for the product Xtra (NDC 51628-4439). 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, do not use, avoid contact with eyes., do not ingest, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Uses
for handwashing, to reduce bacteria on skin
Warnings
For external use only.
Keep Out Of Reach Of Children
Keep out of reach of children
Do Not Use
Do not use with chlorine bleach to avoid irritating fumes.
Avoid Contact With Eyes.
If eye contact occures fush thoroughly with water.
Do Not Ingest
Do not ingest. If ingested, drink plenty of water, contact a physician.
Storage And Handling
Store in a cool and dry pleace, and avoid direct sunlight.
Directions
Spray to wet hand. Scrub and rinse thoroughly.
Inactive Ingredients
Water (Aqua）
Sodium Laureth Sulfate
Decyl Glucoside
Citric Acid
Methylisothiazlione
Phenoxyethanol
Sodium Benzoate
Fragrance
Package Label.Principal Display Panel
Label (Label)
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