| READY AMERICA FIRST AID POCKET - 33 PIECES aspirin, ibuprofen, acetaminophen, alcohol, benzalkonium chloride, bacitracin zinc, neomycin sulfate, polymyxin b sulfate kit
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| Product Information |  
| Product Type | HUMAN OTC DRUG | Item Code (Source) | NDC: 52124-4001 |  | 
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| Packaging |  
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |  
| 1 | NDC: 52124-4001-6 | 1  in 1 KIT |  |  |  | 
| 
| Quantity of Parts |  
| Part # | Package Quantity | Total Product Quantity |  
| Part 1 | 1 TUBE | 0.5 g |  
| Part 2 | 1 PACKET | 2 |  
| Part 3 | 1 PACKAGE | 2 |  
| Part 4 | 3 PACKAGE | 1.5 mL |  
| Part 5 | 1 PACKAGE | 2 |  
| Part 6 | 3 PACKAGE | 2.4 mL |  | 
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| Part 1 of 6 |  
| GENUINE TRIPLE ANTIBIOTIC bacitracin zinc,neomycin sulfate,polymyxin b sulfate ointment
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| Product 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 | 400 [iU]  in 1 g |  
| NEOMYCIN SULFATE (UNII: 057Y626693)  (NEOMYCIN - UNII:I16QD7X297) | NEOMYCIN | 5 mg  in 1 g |  
| POLYMYXIN B SULFATE (UNII: 19371312D4)  (POLYMYXIN B - UNII:J2VZ07J96K) | POLYMYXIN B | 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 | 01/09/2013 |  |  | 
| 
| Part 2 of 6 |  
| IBUPROFEN ibuprofen tablet
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| Product Information |  
| Item Code (Source) | NDC: 52124-0009 |  
| Route of Administration | ORAL |  | 
| 
| Active Ingredient/Active Moiety |  
| Ingredient Name | Basis of Strength | Strength |  
| IBUPROFEN (UNII: WK2XYI10QM)  (IBUPROFEN - UNII:WK2XYI10QM) | IBUPROFEN | 200 mg |  | 
|  | 
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| Product Characteristics |  
| Color | white (WHITE) | Score | no score |  
| Shape | ROUND | Size | 10mm |  
| Flavor |  | Imprint Code | 44;352 |  
| Contains |  |  | 
| 
| Packaging |  
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |  
| 1 | NDC: 52124-0009-1 | 2  in 1 PACKET |  |  |  | 
|  | 
| 
| Marketing Information |  
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |  
| ANDA | ANDA075010 | 01/09/2013 |  |  | 
| 
| Part 3 of 6 |  
| NON-ASPIRIN acetaminophen tablet
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| Product Information |  
| Item Code (Source) | NDC: 52124-0010 |  
| Route of Administration | ORAL |  | 
| 
| Active Ingredient/Active Moiety |  
| Ingredient Name | Basis of Strength | Strength |  
| ACETAMINOPHEN (UNII: 362O9ITL9D)  (ACETAMINOPHEN - UNII:362O9ITL9D) | ACETAMINOPHEN | 325 mg |  | 
|  | 
| 
| Product Characteristics |  
| Color | white (White) | Score | no score |  
| Shape | ROUND | Size | 11mm |  
| Flavor |  | Imprint Code | AZ;234 |  
| Contains |  |  | 
| 
| Packaging |  
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |  
| 1 | NDC: 52124-0010-1 | 2  in 1 PACKAGE |  |  |  | 
|  | 
| 
| Marketing Information |  
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |  
| OTC monograph not final | part343 | 01/09/2013 |  |  | 
| 
| Part 4 of 6 |  
| ALCOHOL CLEANSING PAD isopropyl alcohol liquid
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| Product 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 | 01/09/2013 |  |  | 
| 
| Part 5 of 6 |  
| ASPIRIN aspirin tablet
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| Product Information |  
| Item Code (Source) | NDC: 52124-0011 |  
| Route of Administration | ORAL |  | 
| 
| Active Ingredient/Active Moiety |  
| Ingredient Name | Basis of Strength | Strength |  
| ASPIRIN (UNII: R16CO5Y76E)  (ASPIRIN - UNII:R16CO5Y76E) | ASPIRIN | 325 mg |  | 
|  | 
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| Product Characteristics |  
| Color | white (white) | Score | no score |  
| Shape | ROUND | Size | 11mm |  
| Flavor |  | Imprint Code | 44;157;ASPIRIN |  
| Contains |  |  | 
| 
| Packaging |  
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |  
| 1 | NDC: 52124-0011-1 | 2  in 1 PACKAGE |  |  |  | 
|  | 
| 
| Marketing Information |  
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |  
| OTC monograph final | part343 | 01/09/2013 |  |  | 
| 
| Part 6 of 6 |  
| ANTISEPTIC benzalkonium chloride swab
 |  | 
| 
| Product 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 | 1.3 mg  in 1 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 | 09/09/2010 |  |  | 
|  | 
| 
| Marketing Information |  
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |  
| OTC monograph not final | part333B | 01/09/2013 |  |  |