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REGENECARE HA
REGENECARE HA - 66977-107-25 - (lidocaine HCl)
Drug Information of REGENECARE HA
| Product NDC: | 66977-107 |
| Proprietary Name: | REGENECARE HA |
| Non Proprietary Name: | lidocaine HCl |
| Active Ingredient(s): | 20 mg/g & nbsp; lidocaine HCl |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of REGENECARE HA
| Product NDC: | 66977-107 |
| Labeler Name: | MPM Medical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20070105 |
Package Information of REGENECARE HA
| Package NDC: | 66977-107-25 |
| Package Description: | 4 g in 1 TUBE (66977-107-25) |
NDC Information of REGENECARE HA
| NDC Code | 66977-107-25 |
| Proprietary Name | REGENECARE HA |
| Package Description | 4 g in 1 TUBE (66977-107-25) |
| Product NDC | 66977-107 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | lidocaine HCl |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20070105 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | MPM Medical, Inc. |
| Substance Name | LIDOCAINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
