4342 FIRST AID KIT
4342 first aid kit kit |
Product Information |
Product Type | HUMAN OTC DRUG | Item Code (Source) | NDC: 0498-4342 |
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Packaging |
# | Item Code | Package Description | Marketing Start Date | Marketing End Date |
1 | NDC: 0498-4342-01 | 1 in 1 KIT; Type 0: Not a Combination Product | 10/18/2018 | |
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Quantity of Parts |
Part # | Package Quantity | Total Product Quantity |
Part 1 | 1 PACKET | 2 |
Part 2 | 6 POUCH | 2.4 mL |
Part 3 | 1 PACKET | 2 |
Part 4 | 2 PACKET | 1.8 g |
Part 5 | 3 PACKET | 4.2 mL |
Part 6 | 1 POUCH | 0.4 mL |
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Part 1 of 6 |
AYPANAL EX
acetaminophen tablet |
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Product Information |
Item Code (Source) | NDC: 0498-2110 |
Route of Administration | ORAL |
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Active Ingredient/Active Moiety |
Ingredient Name | Basis of Strength | Strength |
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) | ACETAMINOPHEN | 500 mg |
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Product Characteristics |
Color | white | Score | no score |
Shape | ROUND | Size | 12mm |
Flavor | | Imprint Code |
FR1
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Contains | |
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Packaging |
# | Item Code | Package Description | Marketing Start Date | Marketing End Date |
1 | NDC: 0498-2110-01 | 2 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 | part343 | 01/02/2017 | |
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Part 2 of 6 |
ALCOHOL WIPE
isopropyl alcohol swab |
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Product Information |
Item Code (Source) | NDC: 0498-0143 |
Route of Administration | TOPICAL |
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Active Ingredient/Active Moiety |
Ingredient Name | Basis of Strength | Strength |
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) | ISOPROPYL ALCOHOL | 0.7 mL 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: 0498-0143-04 | 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 | part333A | 09/18/2018 | |
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Part 3 of 6 |
ASPIRIN
aspirin tablet |
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Product Information |
Item Code (Source) | NDC: 0498-0114 |
Route of Administration | ORAL |
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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 | Score | 2 pieces |
Shape | ROUND | Size | 10mm |
Flavor | | Imprint Code |
FR21
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Contains | |
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Packaging |
# | Item Code | Package Description | Marketing Start Date | Marketing End Date |
1 | NDC: 0498-0114-01 | 2 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 | part343 | 09/18/2018 | |
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Part 4 of 6 |
NEOMYCIN
antibiotic ointment |
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Product Information |
Item Code (Source) | NDC: 0498-0730 |
Route of Administration | TOPICAL |
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Active Ingredient/Active Moiety |
Ingredient Name | Basis of Strength | Strength |
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) | NEOMYCIN SULFATE | 3.5 mg in 1 g |
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Inactive Ingredients |
Ingredient Name | Strength |
PETROLATUM (UNII: 4T6H12BN9U) | |
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Packaging |
# | Item Code | Package Description | Marketing Start Date | Marketing End Date |
1 | NDC: 0498-0730-01 | 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 | 03/31/2010 | |
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Part 5 of 6 |
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 6 of 6 |
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 | | 10/18/2018 | |
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