| Product NDC: | 58232-0751 |
| Proprietary Name: | Childrens Benadryl Itch Cooling |
| Non Proprietary Name: | CAMPHOR (SYNTHETIC) |
| Active Ingredient(s): | 4.5 mg/g & nbsp; CAMPHOR (SYNTHETIC) |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 58232-0751 |
| Labeler Name: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120427 |
| Package NDC: | 58232-0751-3 |
| Package Description: | 85 g in 1 TUBE (58232-0751-3) |
| NDC Code | 58232-0751-3 |
| Proprietary Name | Childrens Benadryl Itch Cooling |
| Package Description | 85 g in 1 TUBE (58232-0751-3) |
| Product NDC | 58232-0751 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CAMPHOR (SYNTHETIC) |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20120427 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | CAMPHOR (SYNTHETIC) |
| Strength Number | 4.5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |