Label: ZEP PROFESSIONAL E-2 HAND CLEANER- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 66949-112-01, 66949-112-24 - Packager: Zep 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 December 5, 2013
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- DO NOT USE
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WHEN USING
When using this product
- Do not use in or around eyes. If eye contact occurs, rinse well with water for at least 15 minutes. Consult a physician.
- Do no swallow this product. If swallowed, do not induce vomiting. If individual is conscious, give large quantities of water to drink and consult a physician immediately.
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ZEP PROFESSIONAL E-2 HAND CLEANER
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66949-112 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE .013 g in 10 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) DIDECYLDIMETHYLAMMONIUM CHLORIDE (UNII: JXN40O9Y9B) PEG-6 COCAMIDE (UNII: YZ6NLA4O1E) ALCOHOL (UNII: 3K9958V90M) HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16) DMDM HYDANTOIN (UNII: BYR0546TOW) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) GLUTARAL (UNII: T3C89M417N) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66949-112-01 1000 mL in 1 BOTTLE, PLASTIC 2 NDC:66949-112-24 3785 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/07/2009 Labeler - Zep Inc. (030471374) Establishment Name Address ID/FEI Business Operations Zep Inc. 030471374 manufacture(66949-112)