Label: ANTI-BACTERIAL MULTI-PURPOSE CLEANING WIPES cloth
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Contains inactivated NDC Code(s)
NDC Code(s): 33592-030-30 - Packager: Publishers Clearing House 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 August 3, 2020
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- When using
- Do not use
- Stop use
- Keep out of reach of children
- Indications & usage
- Directions
- Warnings
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Other information
Open pouch by peeling back seal on front of pouch. Do not peel seal all the way off. Remove wipe from center of the pouch, ready to use. As wipe becomes soiled, refold and continue.Reseal pouch to retain moisture.Dispose of used wipes in trash.Do not discard wipes in toilet.Store wipes at temperatures between 50℉ and 90℉.Storage at extreme temperatures may reduce product performance.
- Inactive ingredient
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Description
Open pouch by peeling back seal on front of pouch. Do not peel seal all the way off. Remove wipe from center of the pouch, ready to use. As wipe becomes soiled, refold and continue.Reseal pouch to retain moisture.Dispose of used wipes in trash.Do not discard wipes in toilet.Store wipes at temperatures between 50℉ and 90℉.Storage at extreme temperatures may reduce product performance.
- Package label. Principal display panel
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INGREDIENTS AND APPEARANCE
ANTI-BACTERIAL MULTI-PURPOSE CLEANING WIPES
anti-bacterial multi-purpose cleaning wipes clothProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:33592-030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.4 mL in 100 BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 150 mg in 100 BRONOPOL (UNII: 6PU1E16C9W) (BRONOPOL - UNII:6PU1E16C9W) BRONOPOL 50 mg in 100 METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) (METHYLCHLOROISOTHIAZOLINONE - UNII:DEL7T5QRPN) METHYLCHLOROISOTHIAZOLINONE 0.9 mg in 100 METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) (METHYLISOTHIAZOLINONE - UNII:229D0E1QFA) METHYLISOTHIAZOLINONE 0.3 mg in 100 Inactive Ingredients Ingredient Name Strength DECYL GLUCOSIDE (UNII: Z17H97EA6Y) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:33592-030-30 30 in 1 PACKAGE; Type 0: Not a Combination Product 07/01/2020 
Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 07/01/2020 Labeler - Publishers Clearing House LLC (002633592) Registrant - Wenzhou Guanshang Paper Co., Ltd (412940960) Establishment Name Address ID/FEI Business Operations Wenzhou Guanshang Paper Co., Ltd 412940960 manufacture(33592-030)
