| 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 |