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Pain Relief
Pain Relief - 61010-8100-2 - (benzocaine)
Drug Information of Pain Relief
| Product NDC: | 61010-8100 |
| Proprietary Name: | Pain Relief |
| Non Proprietary Name: | benzocaine |
| Active Ingredient(s): | 200 mg/g & nbsp; benzocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pain Relief
| Product NDC: | 61010-8100 |
| Labeler Name: | Safetec of America, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100501 |
Package Information of Pain Relief
| Package NDC: | 61010-8100-2 |
| Package Description: | .5 g in 1 PACKET (61010-8100-2) |
NDC Information of Pain Relief
| NDC Code | 61010-8100-2 |
| Proprietary Name | Pain Relief |
| Package Description | .5 g in 1 PACKET (61010-8100-2) |
| Product NDC | 61010-8100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzocaine |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100501 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Safetec of America, Inc. |
| Substance Name | BENZOCAINE |
| Strength Number | 200 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
