Product NDC: | 52124-0118 |
Proprietary Name: | Auto 157 |
Non Proprietary Name: | BENZALKONIUM CHLORIDE, LIDOCAINE, BENZOCAINE, ALCOHOL, IBUPROFEN, ACETAMINOPHEN, ASPIRIN |
Active Ingredient(s): | & nbsp; BENZALKONIUM CHLORIDE, LIDOCAINE, BENZOCAINE, ALCOHOL, IBUPROFEN, ACETAMINOPHEN, ASPIRIN |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52124-0118 |
Labeler Name: | Genuine First Aid LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100507 |
Package NDC: | 52124-0118-1 |
Package Description: | 1 KIT in 1 KIT (52124-0118-1) * .9 g in 1 PACKAGE (52124-0004-1) * .8 mL in 1 PACKAGE (52124-0001-1) * .5 mL in 1 PACKAGE (52124-0008-1) * 2 TABLET in 1 PACKAGE (52124-0009-1) * 2 TABLET in 1 PACKAGE (52124-0010-1) * 2 TABLET in 1 PACKAGE (52124-0011-1) |
NDC Code | 52124-0118-1 |
Proprietary Name | Auto 157 |
Package Description | 1 KIT in 1 KIT (52124-0118-1) * .9 g in 1 PACKAGE (52124-0004-1) * .8 mL in 1 PACKAGE (52124-0001-1) * .5 mL in 1 PACKAGE (52124-0008-1) * 2 TABLET in 1 PACKAGE (52124-0009-1) * 2 TABLET in 1 PACKAGE (52124-0010-1) * 2 TABLET in 1 PACKAGE (52124-0011-1) |
Product NDC | 52124-0118 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZALKONIUM CHLORIDE, LIDOCAINE, BENZOCAINE, ALCOHOL, IBUPROFEN, ACETAMINOPHEN, ASPIRIN |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20100507 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Genuine First Aid LLC |
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Strength Number | |
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