Label: MERTHIOLATE- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 0395-9122-92 - Packager: Humco Holding Group, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated June 20, 2020
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- Official Label (Printer Friendly)
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SPL UNCLASSIFIED SECTIONDrug Facts
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Active IngredientBenzalkonium chloride 0.13%
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PurposeAntiseptic
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Usesfirst aid to help prevent skin infection in minor cuts, scrapes, burns and insect bites.
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WarningsFor external use only
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Ask a doctor before use if you havedeep or puncture wounds, animal bites, serious burns.
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When using this productdo not get into eyes. If contact occurs, rinse eyes throughly with water. do not apply over large areas of the body. do not use over raw surfaces or blistered areas. do not use longer than 1 week ...
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Stop use and aska doctor ifcondition persists or gets worse. symptoms clear up and occur again within a few days.
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Keep out of reach of childrenIf swallowed, get medical help or contact a Poison Control Center immediately.
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Directionsadults and children 2 years and older. clean the affected area. apply a small amount on the area 1 to 3 times daily. may be covered with a sterile bandage. if bandaged, let it dry first. children ...
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Inactive ingredientsAlcohol 10%, Acetone, FD&C Red No 4, purified water
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Quality Choice Label
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Premier Value
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DDM
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CVS Label
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Vida Mia Label
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INGREDIENTS AND APPEARANCEProduct Information