Product NDC: | 47682-225 |
Proprietary Name: | Lidocaine Hydrochloride |
Non Proprietary Name: | Lidocaine Hydrochloride |
Active Ingredient(s): | 20 g/L & nbsp; Lidocaine Hydrochloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 47682-225 |
Labeler Name: | Unifirst First Aid Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130412 |
Package NDC: | 47682-225-17 |
Package Description: | .09 L in 1 BOTTLE, SPRAY (47682-225-17) |
NDC Code | 47682-225-17 |
Proprietary Name | Lidocaine Hydrochloride |
Package Description | .09 L in 1 BOTTLE, SPRAY (47682-225-17) |
Product NDC | 47682-225 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Lidocaine Hydrochloride |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20130412 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Unifirst First Aid Corporation |
Substance Name | LIDOCAINE HYDROCHLORIDE |
Strength Number | 20 |
Strength Unit | g/L |
Pharmaceutical Classes |