Label: GO WIPES- benzalkonium chloride cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 50183-112-11 - Packager: American Hygiene Industries
- 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 July 8, 2010
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- Official Label (Printer Friendly)
- DESCRIPTION
- ACTIVE INGREDIENT
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WARNINGS
Warnings
- For external use only
- Do not use if you are allergic to any of the ingredients
- When using this product do not get into eyes. If contact occurs, rinse thoroughly with water.
- Discontinue use if irritation or redness develops if condition persists for more than 72 hours consult a physician
- Keep out of reach of children unless under adult supervision. If swallowed get medical help or contact a Poison Control Center immediately.
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GO WIPES
benzalkonium chloride clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50183-112 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength benzalkonium chloride (UNII: F5UM2KM3W7) (benzalkonium - UNII:7N6JUD5X6Y) benzalkonium chloride 3.480 g in 34.8 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50183-112-11 10 in 1 POUCH 1 3.48 g in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 07/01/2010 Labeler - American Hygiene Industries (102529448)