Label: REFRESH ANTIBAC FOAM- benzalkonium chloride soap
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NDC Code(s):
11084-010-01,
11084-010-05,
11084-010-12,
11084-010-20, view more11084-010-27, 11084-010-40, 11084-010-55, 11084-010-66, 11084-010-96
- Packager: SC Johnson Professional USA, 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 9, 2022
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL - 1 L Bottle Label
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INGREDIENTS AND APPEARANCE
REFRESH ANTIBAC FOAM
benzalkonium chloride soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11084-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 1 L Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT) SALICYLIC ACID (UNII: O414PZ4LPZ) D&C GREEN NO. 5 (UNII: 8J6RDU8L9X) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11084-010-40 0.4 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/12/2017 2 NDC:11084-010-27 1 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/12/2017 3 NDC:11084-010-12 1.2 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/12/2017 4 NDC:11084-010-20 2 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/12/2017 5 NDC:11084-010-05 3.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/12/2017 6 NDC:11084-010-01 0.047 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/27/2019 7 NDC:11084-010-55 208.2 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product 02/27/2019 8 NDC:11084-010-96 0.296 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/01/2019 9 NDC:11084-010-66 1 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/31/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/12/2017 Labeler - SC Johnson Professional USA, Inc. (607378015) Establishment Name Address ID/FEI Business Operations APEX International, Inc. 015226132 manufacture(11084-010) Establishment Name Address ID/FEI Business Operations SC Johnson Professional CA Inc. 203765300 MANUFACTURE(11084-010)