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DRUG FACTS
Antibacterial Lotiontissue
FDA Label NDC 52489-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Imperial Palace Commodity (shenzhen) Co., Ltd for the product Antibacterial Lotiontissue (NDC 52489-003). 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 other, active ingredient(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient(S)
Benzalkonium chloride 0.13%
Purpose
Antiseptic
Use
To help reduce bacteria on the skin that potentially can cause disease.
Warnings
For external use only.
Do Not Use
Do not use if you are allergic to any of the ingredients.
Otc - When Using
When using this product avoid contacting with eyes. In case of eye contact rinse eyes thoroughly with water.
Otc - Stop Use
Stop Use and ask a doctor if irritation or rash occurs. These may be signs of serious condition.
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
Apply to face, nose and hands. Discard after use.
Children under 6 years of age should be supervised when using this product.
How To Uses
Bag
Tear off the middle line of the bag and open the bag then take out of one sheet to use.Dispose the tissue to the trash bin after wiping.
Box
Open the box, take out of tissue as required.
Dispose it to the trash bin after use.
Inactive Ingredients
Water, Glycerin, Aloe Barbadensis leaf extract.
Package Label - Principal Display Panel
NDC:52489-003-01
NDC:52489-003-02
NDC:52489-003-03
* Please review the disclaimer below.
