Label: HAND SANITIZER- benzalkonium chloride gel
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Contains inactivated NDC Code(s)
NDC Code(s): 78522-103-00 - Packager: Northmed
- Category: HUMAN OTC DRUG LABEL
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 March 24, 2021
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- Official Label (Printer Friendly)
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Active IngredientBenzalkonium Chloride, .2%. Purpose: Antiseptic
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PurposeAntiseptic
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UseHand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
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WarningsFor external use only.
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Do not usein children less than 2 months of age - on open skin wounds
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WHEN USINGWhen using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash occurs. These ...
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STOP USEStop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
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KEEP OUT OF REACH OF CHILDRENKeep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
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DirectionsApply a small amount of gel to the hands and massage. Wait for it to dry. The exposure time is 15-30 seconds. Supervise children under 6 years of age when using this product to avoid ...
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Other informationStore between 41-80F (5-27C). Avoid freezing and excessive heat above 104F (40C).
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Inactive ingredientsWater. glycerin, panthenol, aloe vera, hydroxyethyl cellulose, tetrasodium glutamate diacetate, fragrance, chamomile extract, birch leaf extract, elderberry extract
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Package Label - Principal Display Panel(What is this?)4L NDC: 78522-101-01
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INGREDIENTS AND APPEARANCEProduct Information