Label: RADIANCE ANTIBACTERIAL CITRUS SCENT HAND- chloroxylenol soap
- NDC Code(s): 73487-004-01, 73487-004-02, 73487-004-03
- Packager: Korex Chicago LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 16, 2023
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- Drug Facts
- Active ingredient
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- Inactive ingredients
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SPL UNCLASSIFIED SECTION
LEAVES DISHES CLEAN
TOUGH ON GREASE
COMPARE TO DAWN ULTRA ANTIBACTERIAL HAND SOAP ORANGE SCENT*
CITRUS SCENT
Ultra Concentrated Dishwashing Liquid
DIST. & SOLD EXCLUSIVELY BY: ALDI BATAVIA, IL 60510
ALDI Twice as Nice GUARANTEE
- item replaced
- money refunded
*This product is not manufactured or distributed by Procter & Gamble, distributor of Dawn Ultra Antibacterial Hand Soap Orange Scent
Do not add bleach. Not for use in dishwashers.
Product Not Tested on Animals
www.aldi.us or call 800-325-7894
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INGREDIENTS AND APPEARANCE
RADIANCE ANTIBACTERIAL CITRUS SCENT HAND
chloroxylenol soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73487-004 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) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U) Product Characteristics Color Score Shape Size Flavor CITRUS Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73487-004-01 573 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/01/2020 12/02/2022 2 NDC:73487-004-02 709 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/25/2021 3 NDC:73487-004-03 828 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/25/2022 11/30/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 01/01/2020 Labeler - Korex Chicago LLC (792133147) Establishment Name Address ID/FEI Business Operations Korex Chicago LLC 792133147 manufacture(73487-004)