Label: AMERICAN RED CROSS FIRST AID KIT- alcohol, benzalkonium chloride, bacitracin zinc, neomycin sulfate, polymyxin b sulfate, alcohol kit
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Contains inactivated NDC Code(s)
NDC Code(s): 42354-7482-4, 52124-0001-1, 52124-0002-1, 52124-0003-1, view more52124-2906-1 - Packager: Tomy International
- 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 January 17, 2012
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- Active Ingredient
- Use
- Warnings
- STORAGE AND HANDLING
- Do not use:
- STOP USE
- Keep out of reach of children
- WHEN USING
- Inactive Ingredient
- DESCRIPTION
- PRINCIPAL DISPLAY PANEL
- Active Ingredient
- Uses:
- Warnings>
- Do not use
- Stop use and consult a doctor
- Keep out of reach of children
- Directions
- Other Information
- PRINCIPAL DISPLAY PANEL
- Active Ingredint
- Use
- Warning
- Keep out of reach of children
- STOP USE
- DO NOT USE
- WHEN USING
- Inactive Ingredient
- DESCRIPTION
- Active Ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive Ingredients
- Keep out of reach of children
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AMERICAN RED CROSS FIRST AID KIT
alcohol, benzalkonium chloride, bacitracin zinc, neomycin sulfate, polymyxin b sulfate, alcohol kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:42354-7482 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42354-7482-4 1 in 1 KIT Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 2 TUBE 1.0 g Part 2 2 PACKAGE 1.6 mL Part 3 4 PACKAGE 2.0 mL Part 4 2 PACKET 1.8 g Part 1 of 4 GENUINE TRIPLE ANTIBIOTIC
bacitracin zinc,neomycin sulfate,polymyxin b sulfate ointmentProduct Information Item Code (Source) NDC:52124-0003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN ZINC 400 [iU] in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 5 mg in 1 g POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B SULFATE 5000 [iU] in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52124-0003-1 .5 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333B 01/11/2011 Part 2 of 4 ANTISEPTIC TOWELETTE
benzalkonium chloride swabProduct Information Item Code (Source) NDC:52124-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.40 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52124-0001-1 0.8 mL in 1 PACKAGE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333E 01/11/2011 Part 3 of 4 ALCOHOL CLEANSING PAD
isopropyl alcohol liquidProduct Information Item Code (Source) NDC:52124-0002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52124-0002-1 0.5 mL in 1 PACKAGE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/11/2011 Part 4 of 4 GENUINE HAND SANITIZER
alcohol gelProduct Information Item Code (Source) NDC:52124-2906 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 g in 100 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52124-2906-1 0.9 g in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/28/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/17/2012 Labeler - Tomy International (065183758)