Label: REDI WIPES- benzalkonium chloride patch
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Contains inactivated NDC Code(s)
NDC Code(s): 52553-003-50 - Packager: Radienz Living, LLC
- 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 March 16, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do Not Use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
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Directions:
Take wipe and rub thoroughly over all surfaces of both hands. Rub hands together briskly to dry. Dispose of wipe. Do not flush.
Lift tab at front of lid to open. Pull up corner of center sheet and thread through dispenser slit in the lid. Pull out exposed wipe at 45º angle and snap off. The next wipe is ready for dispensing. Close lid to retain moisture. Dispose of used wipe in trash. Do not flush.
- Inactive ingredients
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Other Information
*Kills 99.9% of germs that may cause illness, including E. Coli and MRSA in just 15 seconds.
RediWipes™ Antibacterial Wipes are made with a soothing pH balanced formula that kills germs and leaves your skin feeling clean and soft.
They are a smart solution for fast cleanups anywhere soap and water are not available. Use them at school, work or sporting events. Can also be used when cleaning up the car or boat.RediWipes logo™, Free Of logo™, and Wind Energy/Artesian Glacial Aquifer Water logo™ are trademarks of U.S. Nonwovens Corp.
All rights reserved.
**This product is not manufactured or distributed by Edgewell Personal Care, owner of the registered trademark, Wet Ones®.
DISTRIBUTED BY: U.S. NONWOVENS CORP. 100 EMJAY BLVD., BRENTWOOD, NY 11717 - Principal Display Panel
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INGREDIENTS AND APPEARANCE
REDI WIPES
benzalkonium chloride patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52553-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.115 mg in 100 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T) DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1) GLYCERETH-2 (UNII: 0UY833L6XU) ALOE VERA LEAF (UNII: ZY81Z83H0X) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52553-003-50 50 in 1 PACKAGE 03/16/2021 1 0.115 mg in 1 PATCH; Type 1: Convenience Kit of Co-Package Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/16/2021 Labeler - Radienz Living, LLC (117451061) Registrant - Radienz Living, LLC (080453184) Establishment Name Address ID/FEI Business Operations Radienz Living, LLC 080453184 manufacture(52553-003)
