Active Ingredients
Benzalkonium chloride
Ethyl Alcohol
Bcp
FDA Label NDC 78502-7000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Belskin S. De, R.l. De C.v for the product Bcp (NDC 78502-7000). 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, inactive ingredients, warnings and precautions, warnings, dosage and administration, purpose, stop use, 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
Inactive Ingredients
WATER, ALOE VERA LEAF, ANHYDROUS CITRIC ACID, DIMETHICONE, GLYCERIN, EDETATE SODIUM TETRAHYDRATE, ALPHA TOCOPHEROL ACETATE, HYDANTOIN, POLYSORBATE 20, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE
Warnings And Precautions
Children under 6 years of age should be supervised when using.
If swallowed, get medical help or contact a Poison Control Center right away.
Warnings
For external use only. Flammable. Keep away from heat or flame
Dosage And Administration
APPLY TO HANDS AND ALLOW TO DRY WITHOUT WIPING.
Purpose
ANTIBACTERIAL
Stop Use
STOP USE AND ASK A DOCTOR IF IRRITATION OR RASH DEVELOPS AND CONTINUES FOR MORE THAN 72 HOURS.
Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Indications And Usage
APPLY TO HANDS AND ALLOW TO DRY WITHOUT WIPING.
* Please review the disclaimer below.
