Label: E2 ANTIBACTERIAL FOAMING SKIN CLEANSER- benzalkonium chloride soap
- NDC Code(s): 65601-817-03, 65601-817-04, 65601-817-29
- Packager: Betco Corporation, Ltd.
- 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 September 11, 2020
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- E2 Antibacterial Foaming Skin Cleanser
- E2 Antibacterial Foaming Skin Cleanser
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E2 Antibacterial Foaming Skin Cleanser
Warnings
- For external use only.
- When using this product avoid contact with eyes. In case of contact flush with water
- Discontinue use is irritation or redness develops.
- Stop use and ask a doctor If irritation persists for more than 72 hours, or if condition persists for more than 72 hours.
- KEEP OUT OF REACH OF CHILDREN.
- If swallowed, get medical help or contact Poison Control Center right away.
- E2 Antibacterial Foaming Skin Cleanser
- E2 Antibacterial Foaming Skin Cleanser
- E2 Antibacterial Foaming Skin Cleanser
- E2 Antibacterial Foaming Skin Cleanser
- E2 Antibacterial Foaming Skin Cleanser
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INGREDIENTS AND APPEARANCE
E2 ANTIBACTERIAL FOAMING SKIN CLEANSER
benzalkonium chloride soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65601-817 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 mL Inactive Ingredients Ingredient Name Strength CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) WATER (UNII: 059QF0KO0R) LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65601-817-04 3780 mL in 1 JUG; Type 0: Not a Combination Product 01/17/2014 2 NDC:65601-817-29 1000 mL in 1 BAG; Type 0: Not a Combination Product 01/17/2014 3 NDC:65601-817-03 750 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/17/2014 09/11/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/17/2014 Labeler - Betco Corporation, Ltd. (024492831) Registrant - Betco corporation, Ltd. (024492831) Establishment Name Address ID/FEI Business Operations Betco Corporation, Ltd. 005050158 manufacture(65601-817) Establishment Name Address ID/FEI Business Operations Betco Corportation, Ltd. 024492831 label(65601-817) , pack(65601-817) , manufacture(65601-817)