Label: FOAMING HAND SANITIZER WITH ALOE- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 63148-240-08 - Packager: APOLLO HEALTH AND BEAUTY CARE
- 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 25, 2010
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INGREDIENTS AND APPEARANCE
FOAMING HAND SANITIZER WITH ALOE
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63148-240 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1000 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63148-240-08 236 mL in 1 BOTTLE, PUMP Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333 06/25/2010 Labeler - APOLLO HEALTH AND BEAUTY CARE (201901209)