4167 FIRST AID KIT
4167 first aid kit |
| Product Information |
| Product Type | HUMAN OTC DRUG | Item Code (Source) | NDC: 0498-4167 |
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| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 0498-4167-01 | 1 in 1 KIT | 09/13/2018 | |
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| Quantity of Parts |
| Part # | Package Quantity | Total Product Quantity |
| Part 1 | 6 PACKET | 21 g |
| Part 2 | 1 BOTTLE | 30 mL |
| Part 3 | 20 PACKET | 18 g |
| Part 4 | 4 PACKET | 5.6 mL |
| Part 5 | 10 POUCH | 4 mL |
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| Part 1 of 5 |
BURN JEL
gel for burns gel |
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| Product Information |
| Item Code (Source) | NDC: 0498-0203 |
| Route of Administration | TOPICAL |
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| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) | LIDOCAINE HYDROCHLORIDE ANHYDROUS | 2 g in 100 g |
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| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 0498-0203-00 | 3.5 g in 1 PACKET; Type 0: Not a Combination Product | | |
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| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC monograph not final | part348 | 09/19/2018 | |
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| Part 2 of 5 |
EYESALINE EMERGENCY EYEWASH
purified water liquid |
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| Product Information |
| Item Code (Source) | NDC: 0498-0100 |
| Route of Administration | OPHTHALMIC |
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| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) | WATER | 98.6 mL in 100 mL |
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| Inactive Ingredients |
| Ingredient Name | Strength |
| SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74) | |
| SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN) | |
| SODIUM CHLORIDE (UNII: 451W47IQ8X) | |
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| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 0498-0100-01 | 30 mL in 1 BOTTLE; Type 0: Not a Combination Product | | |
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| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC monograph final | part349 | 12/18/2018 | |
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| Part 3 of 5 |
TRIPLE ANTIBIOTIC
bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointment |
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| Product Information |
| Item Code (Source) | NDC: 0498-0750 |
| Route of Administration | TOPICAL |
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| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) | POLYMYXIN B | 5000 [iU] in 1 g |
| BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) | BACITRACIN | 400 [iU] in 1 g |
| NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) | NEOMYCIN | 3.5 mg in 1 g |
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| Inactive Ingredients |
| Ingredient Name | Strength |
| PETROLATUM (UNII: 4T6H12BN9U) | |
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| Product Characteristics |
| Color | white | Score | |
| Shape | | Size | |
| Flavor | | Imprint Code | |
| Contains | |
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| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 0498-0750-35 | 0.9 g in 1 PACKET; Type 0: Not a Combination Product | | |
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| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC monograph final | part333B | 09/19/2018 | |
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| Part 4 of 5 |
ANTISEPTIC TOWELETTE
benzalkonium chloride liquid |
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| Product Information |
| Item Code (Source) | NDC: 0498-0501 |
| Route of Administration | TOPICAL |
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| 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 |
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| Inactive Ingredients |
| Ingredient Name | Strength |
| WATER (UNII: 059QF0KO0R) | |
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| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 0498-0501-00 | 1.4 mL in 1 PACKET; Type 0: Not a Combination Product | | |
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| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC monograph not final | part333E | 12/22/2017 | |
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| Part 5 of 5 |
STING RELIEF PAD
ethyl alcohol, lidocaine swab |
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| Product Information |
| Item Code (Source) | NDC: 0498-0733 |
| Route of Administration | TOPICAL |
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| Active Ingredient/Active Moiety |
| Ingredient Name | Basis of Strength | Strength |
| LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) | LIDOCAINE HYDROCHLORIDE ANHYDROUS | 20 mg in 1 mL |
| ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) | ALCOHOL | 0.5 mL in 1 mL |
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| Packaging |
| # | Item Code | Package Description | Marketing Start Date | Marketing End Date |
| 1 | NDC: 0498-0733-00 | 0.4 mL in 1 POUCH; Type 0: Not a Combination Product | | |
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| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| OTC monograph not final | part348 | 12/23/2017 | |
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| Marketing Information |
| Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
| unapproved drug other | | 09/13/2018 | |
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