Label: BODY PRESCRIPTIONS ANTIBACTERIAL WIPES ALOE SCENTED LEMON SCENTED FRESH CITRUS SCENTED- benzalkonium chloride kit
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Contains inactivated NDC Code(s)
NDC Code(s): 50563-221-01, 50563-222-01, 50563-223-01, 50563-224-01 - Packager: ENCHANTE ACCESSORIES INC.
- Category: HUMAN OTC DRUG LABEL
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 June 14, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- BODY PRESCRIPTIONS ANTIBACTERIAL HAND WIPES ALOE SCENTED
- Use
- WARNINGS
- Directions
- Inactive ingredients
- BODY PRESCRIPTIONS ANTIBACTERIAL HAND WIPES LEMON SCENTED
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- Warnings
- Stop Use
- Keep out of reach of children
- Directions
- Inactive Ingredients
- BODY PRESCRIPTIONS ANTIBACTERIAL HAND WIPES FRESH CITRUS SCENTED
- Active Ingredient
- Purpose
- Uses
- Warnings
- Stop Use
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Inactive Ingredients
- BODY PRESCRIPTIONS ANTIBACTERIAL HAND WIPES ALOE SCENTED
- BODY PRESCRIPTIONS ANTIBACTERIAL HAND WIPES LEMON SCENTED
- BODY PRESCRIPTIONS ANTIBACTERIAL HAND WIPES FRESH CITRUS SCENTED
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INGREDIENTS AND APPEARANCE
BODY PRESCRIPTIONS ANTIBACTERIAL WIPES ALOE SCENTED LEMON SCENTED FRESH CITRUS SCENTED
benzalkonium chloride kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50563-224 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50563-224-01 1 in 1 KIT 06/12/2020 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 PACKET 20 Part 2 1 PACKET 20 Part 3 1 PACKET 20 Part 1 of 3 BODY PRESCRIPTIONS ANTIBACTERIAL WIPES ALOE SCENTED
benzalkonium chloride solutionProduct Information Item Code (Source) NDC:50563-221 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 4.5 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50563-221-01 20 in 1 PACKET; 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 06/12/2020 Part 2 of 3 BODY PRESCRIPTIONS ANTIBACTERIAL WIPES LEMON SCENTED
benzalkonium chloride solutionProduct Information Item Code (Source) NDC:50563-222 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 4.5 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50563-222-01 20 in 1 PACKET; 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 06/12/2020 Part 3 of 3 BODY PRESCRIPTIONS ANTIBACTERIAL WIPES FRESH CITRUS SCENTED
benzalkonium chloride solutionProduct Information Item Code (Source) NDC:50563-223 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 4.5 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50563-223-01 20 in 1 PACKET; 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 06/12/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/12/2020 Labeler - ENCHANTE ACCESSORIES INC. (186050696) Establishment Name Address ID/FEI Business Operations Zhejiang Ruolin Hygienic Products Co., Ltd. 415426870 manufacture(50563-224, 50563-221, 50563-222, 50563-223)