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Drug Facts
Antiseptic
FDA Label NDC 55550-200
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Total Resources International for the product Antiseptic (NDC 55550-200). 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 other, active ingredients, purpose, uses, warnings, otc - do not use, otc - stop use, otc - 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
Active Ingredients
Benzalkonium Chloride 0.13%
Purpose
First Aid Antiseptic
Uses
- Antiseptic cleansing of face, hands and body to decrease bacteria on skin without soap and water
Warnings
For external use only
Otc - Do Not Use
Do not use in the eyes. If this happens, rinse thoroughly with water.
Otc - Stop Use
Stop use and ask doctor if irritation or redness develop and 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
- tear open packet, unfold and use as a washcloth. Allow hands to dry without wiping.
Inactive Ingredients
alcohol, water
Principal Display Panel – Packet Label
NDC 55550-200-00
Antiseptic
Towelette
Benzalkonium Chloride/
First Aid Antiseptic
1 SINGLE-USE
PREMOISTENED TOWELETTE
Principal Display Panel – Packet Label (Tot03 0001 01)
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