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BeeGentle
BeeGentle - 14060-002-02 - (benzocaine)
Drug Information of BeeGentle
| Product NDC: | 14060-002 |
| Proprietary Name: | BeeGentle |
| Non Proprietary Name: | benzocaine |
| Active Ingredient(s): | 210 mg/g & nbsp; benzocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BeeGentle
| Product NDC: | 14060-002 |
| Labeler Name: | CAO Group, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100901 |
Package Information of BeeGentle
| Package NDC: | 14060-002-02 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 PACKAGE (14060-002-02) > 30 g in 1 BOTTLE, PLASTIC |
NDC Information of BeeGentle
| NDC Code | 14060-002-02 |
| Proprietary Name | BeeGentle |
| Package Description | 1 BOTTLE, PLASTIC in 1 PACKAGE (14060-002-02) > 30 g in 1 BOTTLE, PLASTIC |
| Product NDC | 14060-002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | benzocaine |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100901 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | CAO Group, Inc. |
| Substance Name | BENZOCAINE |
| Strength Number | 210 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient] |
