CVS HEALTH ALL PURPOSE KIT
isopropyl alcohol, bacitracin zinc,neomycin sulfate,polymyxin b sulfate, benzocaine kit |
Product Information |
Product Type | HUMAN OTC DRUG | Item Code (Source) | NDC: 69842-419 |
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Packaging |
# | Item Code | Package Description | Marketing Start Date | Marketing End Date |
1 | NDC: 69842-419-01 | 1 in 1 KIT; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product) | 09/01/2019 | |
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Quantity of Parts |
Part # | Package Quantity | Total Product Quantity |
Part 1 | 12 POUCH | 6 mL |
Part 2 | 3 TUBE | 2.7 g |
Part 3 | 3 PACKAGE | 3000 mg |
Part 4 | 2 PACKET | 1.8 g |
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Part 1 of 4 |
EASY CARE FIRST AID SKIN CLEANSING ALCOHOL WIPE
isopropyl alcohol swab |
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Product Information |
Item Code (Source) | NDC: 44224-0010 |
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 | 70 mL in 100 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: 44224-0010-0 | 0.5 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 | 09/02/2019 | |
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Part 2 of 4 |
EASY CARE FIRST AID TRIPLE ANTIBIOTIC
bacitracin zinc,neomycin sulfate,polymyxin b sulfate ointment |
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Product Information |
Item Code (Source) | NDC: 44224-0013 |
Route of Administration | TOPICAL |
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Active Ingredient/Active Moiety |
Ingredient Name | Basis of Strength | Strength |
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) | BACITRACIN ZINC | 400 [iU] in 1 g |
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) | POLYMYXIN B | 5000 [iU] in 1 g |
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) | NEOMYCIN SULFATE | 5 mg in 1 g |
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Inactive Ingredients |
Ingredient Name | Strength |
PETROLATUM (UNII: 4T6H12BN9U) | |
MINERAL OIL (UNII: T5L8T28FGP) | |
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Packaging |
# | Item Code | Package Description | Marketing Start Date | Marketing End Date |
1 | NDC: 44224-0013-4 | 0.9 g in 1 TUBE; 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 | 09/01/2019 | |
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Part 3 of 4 |
AFTER BITE WIPE INSECT STING RELIEF
benzocaine,alcohol swab |
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Product Information |
Item Code (Source) | NDC: 44224-0014 |
Route of Administration | TOPICAL |
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Active Ingredient/Active Moiety |
Ingredient Name | Basis of Strength | Strength |
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) | BENZOCAINE | 6 mg in 100 mg |
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) | ALCOHOL | 60 mg in 100 mg |
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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: 44224-0014-1 | 1000 mg in 1 PACKAGE; 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 | 09/01/2019 | |
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Part 4 of 4 |
EASY CARE FIRST AID AFTERBURN
benzalkonium chloride, lidocaine cream |
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Product Information |
Item Code (Source) | NDC: 44224-0012 |
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 | 0.5 g in 100 g |
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) | BENZALKONIUM CHLORIDE | 0.13 g in 100 g |
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Packaging |
# | Item Code | Package Description | Marketing Start Date | Marketing End Date |
1 | NDC: 44224-0012-1 | 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 not final | part333A | 09/01/2019 | |
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Marketing Information |
Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
unapproved drug other | | 09/01/2019 | |
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