Label: HAND SANITIZER WIPES- alcohol solution
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Contains inactivated NDC Code(s)
NDC Code(s): 77848-001-15, 77848-002-15, 77848-003-15 - Packager: PDD Design 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 December 5, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
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INGREDIENTS AND APPEARANCE
HAND SANITIZER WIPES
alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77848-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 mg in 100 mL Inactive Ingredients Ingredient Name Strength COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N) PLANTAGO MAJOR LEAF (UNII: 7DC28K241X) ETHYLPARABEN (UNII: 14255EXE39) CETRIMONIUM BROMIDE (UNII: L64N7M9BWR) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) PEG-40 CASTOR OIL (UNII: 4ERD2076EF) 2-NITROPROPANE (UNII: GKV234L2QH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77848-003-15 15 mL in 1 CARTON; Type 0: Not a Combination Product 05/29/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/29/2020 HAND SANITIZER WIPES
alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77848-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 mg in 100 mL Inactive Ingredients Ingredient Name Strength PLANTAGO MAJOR LEAF (UNII: 7DC28K241X) ETHYLPARABEN (UNII: 14255EXE39) CETRIMONIUM BROMIDE (UNII: L64N7M9BWR) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PEG-40 CASTOR OIL (UNII: 4ERD2076EF) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77848-001-15 15 mL in 1 PACKET; Type 0: Not a Combination Product 06/03/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/03/2020 HAND SANITIZER WIPES
alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77848-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 mg in 100 mL Inactive Ingredients Ingredient Name Strength COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N) ETHYLPARABEN (UNII: 14255EXE39) CETRIMONIUM BROMIDE (UNII: L64N7M9BWR) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) 2-NITROPROPANE (UNII: GKV234L2QH) LIMONENE, (+)- (UNII: GFD7C86Q1W) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) PANTHENOL (UNII: WV9CM0O67Z) CITRAL (UNII: T7EU0O9VPP) SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77848-002-15 15 mL in 1 PACKET; Type 0: Not a Combination Product 05/29/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/29/2020 Labeler - PDD Design LLC (065947601)