Active Ingredient
Benzalkonium Chloride 0.13% w/w
Omnicide Antimicrobial
FDA Label NDC 69085-466
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Steriweb Medical, Llc for the product Omnicide Antimicrobial (NDC 69085-466). 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, purpose, uses, warnings, ask a doctor before use if you have, when using this product, stop and ask a doctor if, 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
Purpose
First Aid Antiseptic
Uses
First aid to help treat, protect and prevent skin infection associated with
- minor cuts
- scrapes
- burns
Warnings
For external use only
Ask A Doctor Before Use If You Have
- deep or puncture wounds
- animal bites
- serious burns
When Using This Product
- Do not use in or near the eyes
- Do not use if you have a history of allergy to any of the ingredients
Stop And Ask A Doctor If
- condition worsens
- symptoms persist for more than 7 days, or clear up and occur again within a few days.
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
- adults and children 2 years and older: clean the affected area; apply a small amount on the area 1-3 times daily; may be covered with a sterile bandage (let dry first)
- children under 2 years: ask a doctor
Other Information
Avoid excessive heat.
Inactive Ingredients
USP Petrolatum, Water, Polihexanide (PHBM)
Questions?
1-360-448-7881
Package Label.Principal Display Panel
Omnicide30 (Omnicide30)
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