Otc - Active Ingredient
benzalkonium chloride
Youke An
FDA Label NDC 54749-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hunan Zonwe Pharmaceutical Co., Ltd. for the product Youke An (NDC 54749-001). 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, otc - keep out of reach of children, otc - purpose, dosage & administration, indications & usage, inactive ingredient, warnings, 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
Otc - Keep Out Of Reach Of Children
keep out of children
Otc - Purpose
Kills 99.99% of germs
Dosage & Administration
a little
Indications & Usage
It shall be directly sprayed onto skin, wounds, mucosa and infected parts. It can be applied several times a day to bring continuous antiseptic effects on skin surface for lasting protection.
Inactive Ingredient
Propylene glycol
Sodium dihydrogen phosphate dihydrate
Disodium hydrogen phosphate
Disodium edetate, dihydrate
water
Warnings
1.This product is one kind of solution for external use, and is never for internal usage.
2.Activity of this product may be affected by anion surfactant or soap, and cannot be used together.
3.It is forbidden for people who are allergic to this product.
4.Turbidity or deposits may appear at a low temperature. It can be placed in warm waterfor heating, or used after it is dissolved through shaking.
5.It shall be sealed and kept in a dark and dry place.
6.Mucosa disinfection is only used for diagnosis and treatment by a medical institution.
Package Label.Principal Display Panel
Label (Label)
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