Otc - Active Ingredient
Benzalkonium Chloride
Sanipro Disinfectant Wipes
FDA Label NDC 75356-0004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Aj Co., Ltd. for the product Sanipro Disinfectant Wipes (NDC 75356-0004). 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 otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Propylene Glycol
Phenoxyethanol
Glycerin
Sodium Benzoate
Sodium Citrate
Disodium EDTA
Polysorbate 20
Citric Acid
Melaleuca Alternifolia (Tea Tree) Leaf Oil
Tocopheryl Acetate
Otc - Purpose
Antibacterial Wipes to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
Thoroughly wipe hands with wipe.
Discard properly. Not flushable.
Be sure to close lid to keep wipes moist.
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 thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
for external use only
Package Label.Principal Display Panel
Label (Label)
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