| NDC Code | 69968-0625-1 |
|---|
| Package Description | 1 TUBE in 1 CARTON (69968-0625-1) / 28.3 g in 1 TUBE |
|---|
| Product NDC | 69968-0625 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Benadryl Original Strength Itch Stopping |
|---|
| Non-Proprietary Name | Diphenhydramine Hydrochloride And Zinc Acetate |
|---|
| Dosage Form | CREAM |
|---|
| Usage | TOPICAL |
|---|
| Start Marketing Date | 20200131 |
|---|
| Marketing Category Name | OTC MONOGRAPH DRUG |
|---|
| Application Number | M017 |
|---|
| Manufacturer | Kenvue Brands LLC |
|---|
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE |
|---|
| Strength | 10; 1 |
|---|
| Strength Unit | mg/g; mg/g |
|---|
| Pharmacy Classes | Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
|---|