- Active ingredient
- Purpose
- Uses
- Warnings
- DO NOT USE
-
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
-
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)