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Boy Butter
Boy Butter - 24488-042-82 - (Benzocaine)
Drug Information of Boy Butter
| Product NDC: | 24488-042 |
| Proprietary Name: | Boy Butter |
| Non Proprietary Name: | Benzocaine |
| Active Ingredient(s): | 73.9395789 mg/mL & nbsp; Benzocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Boy Butter
| Product NDC: | 24488-042 |
| Labeler Name: | Boy Butter Lubes |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120925 |
Package Information of Boy Butter
| Package NDC: | 24488-042-82 |
| Package Description: | 266 mL in 1 BOTTLE, PUMP (24488-042-82) |
NDC Information of Boy Butter
| NDC Code | 24488-042-82 |
| Proprietary Name | Boy Butter |
| Package Description | 266 mL in 1 BOTTLE, PUMP (24488-042-82) |
| Product NDC | 24488-042 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzocaine |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120925 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Boy Butter Lubes |
| Substance Name | BENZOCAINE |
| Strength Number | 73.9395789 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
