Active Ingredient - Antiseptic
Benzalkonium Chloride 0.13%
The following Structured Product Label (SPL) was submitted to the FDA by Genuine First Aid Llc for the product Antiseptic (NDC 52124-0001). 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 ingredient - antiseptic, purpose - antiseptic, use - antiseptic, warnings, precautions and directions - antiseptic, inactive ingredients - antiseptic, active ingredient - alcohol prep pad, use - alcohol prep pad, warnings, precautions and directions - alcohol prep pad, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Benzalkonium Chloride 0.13%
Antiseptic
For Professional and hospital use. Helps prevent infection. Antiseptic cleansing of face, hands and body without soap and water.
For External use only.
Keep out of Reach of Children.
Stop use if unusual redness, swelling or other symptoms occur, consult a physician immediately.
Do not uses in eyes or over large areas of the body.
Tear open packet, unfold towelette and use to cleanse desired skin area. Discard towelette appropriately after single use.
Purified Water
Isopropyl Alcohol 70%
For preparation of the skin before injection
For External Use Only
Flammable - Keep away from fire or flame
Do Not Use - with electrocautery, in eyes
Stop Use and Ask a Doctor if - Irritation or redness develop and persists for more than 72 hours
Keep out of Reach of Children
If swallowed, get medical help or contact a poison control center right away.
Tear Open packet, unfold and use as and wipe injection site vigorously and discard.
Store at Room Temperature
Keep out of Reach of Children
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