Label: KROGER ANTIBACTERIAL GREEN APPLE HAND- chloroxylenol soap
- NDC Code(s): 73487-001-01, 73487-001-02, 73487-001-03
- Packager: Korex Chicago LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 11, 2023
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- Drug Facts
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- Inactive ingredients
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SPL UNCLASSIFIED SECTION
Kroger®
COMPARE TO DAWN® ULTRA ANTIBACTERIAL HAND SOAP.
2X CLEANING POWER VERSUS NON-CONCENTRATED DISH SOAPS
GREASE CLEANING
ULTRA CONCENTRATED DISH SOAP
Our Brands. Our Guarantee.
Love It or Your Money Back.www.kroger.com
For More Ingredient Information, Visit www.kroger.com or call 800-632-6900
Do not add bleach. Not for use in dishwashers.
Contains surfactants
Phosphate Free
DISTRIBUTED BY THE KROGER CO.
CINCINNATI, OHIO 45202
*Dawn® is a registered trademark of The Procter and Gamble Company, Cincinnati, OH 45202. The Procter and Gamble Company is not affiliated with The Kroger Co. or this product.
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INGREDIENTS AND APPEARANCE
KROGER ANTIBACTERIAL GREEN APPLE HAND
chloroxylenol soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73487-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 0.3 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0) SODIUM LAURYL SULFATE (UNII: 368GB5141J) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Product Characteristics Color Score Shape Size Flavor APPLE (Green Apple) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73487-001-01 709 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/01/2019 05/01/2024 2 NDC:73487-001-02 1770 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2020 3 NDC:73487-001-03 828 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 04/01/2019 Labeler - Korex Chicago LLC (792133147) Establishment Name Address ID/FEI Business Operations Korex Chicago LLC 792133147 manufacture(73487-001)