Antibacterial Lavender Bouquet Liquid
FDA Label NDC 52000-435

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Universal Distribution Center Llc for the product Antibacterial Lavender Bouquet (NDC 52000-435). 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 ​drug facts, active ingredient, purpose, ​use, ​warnings, otc - keep out of reach of children, directions, ​inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

​Drug Facts

Active Ingredient

Benzalkonium chloride 0.13%

Purpose

Antibacterial

​Use

for handwashing to decrease bacteria on the skin

​Warnings

​For external use only

When using this product • avoid contact with eyes ​• in case of eye contact, flush with water

Stop use and ask a doctor if ​• irritation or redness develops • condition persists for more than 72 hours

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

• wet hands and apply soap • lather all surfaces of hands and fingers by rubbing vigorously for at least 20 seconds • rinse hands well and dry

​Inactive Ingredients

Water(Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Cocamide Methyl MEA, Citric Acid, Methylisothiazolinone, Iodopropynyl Butylcarbamate, Fragrance, Sodium Chloride, D&C Red No. 33, FD&C Blue No. 1.

Packaging

Antibacteriallavenderbouquet (52000435 2)

Antibacteriallavenderbouquet (52000435 2)

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