Active Ingredients
Benzalkonium Chloride 0.13%
Benzalkonium Chloride
FDA Label NDC 82663-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Purocor Llc for the product Benzalkonium Chloride (NDC 82663-001). 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 active ingredients, purpose, use(s), warnings, do not use, when using this product, stop use and ask doctor, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use(S)
Hand Sanitizer to help reduce bacteria that potentially can cause disease.
Warnings
For external use only.
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 eyes thoroughly with water.
Stop Use And Ask Doctor
If irritation or rash appears.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Place enough product on hands to cover all surfaces. Rub hands together until dry.
- Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
- Store between 15-30°C (59-86°F)
Inactive Ingredients
Aloe Barbadensis Leaf Extract, Citric Acid, Decyl Glucoside, Disodium EDTA, Fragrance, Phenoxyethanol, Potassium Sorbate, Purified Water, Sodium Benzoate
Principal Display Panel
PuroCor
CLINICAL STRENGTH FORMULA
SANITIZING
WIPES
1200 WET WIPES
Lemon Scent
ALCOHOL
FREE
8" X 5.65" (20.3cm x 14.4cm)
* Please review the disclaimer below.
