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Witch Hazel
Witch Hazel - 49348-805-16 - (Witch Hazel)
Drug Information of Witch Hazel
| Product NDC: | 49348-805 |
| Proprietary Name: | Witch Hazel |
| Non Proprietary Name: | Witch Hazel |
| Active Ingredient(s): | 86 mL/100mL & nbsp; Witch Hazel |
| Administration Route(s): | ORAL; TOPICAL |
| Dosage Form(s): | OIL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Witch Hazel
| Product NDC: | 49348-805 |
| Labeler Name: | Sunmark |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090416 |
Package Information of Witch Hazel
| Package NDC: | 49348-805-16 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (49348-805-16) |
NDC Information of Witch Hazel
| NDC Code | 49348-805-16 |
| Proprietary Name | Witch Hazel |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (49348-805-16) |
| Product NDC | 49348-805 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Witch Hazel |
| Dosage Form Name | OIL |
| Route Name | ORAL; TOPICAL |
| Start Marketing Date | 20090416 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Sunmark |
| Substance Name | WITCH HAZEL |
| Strength Number | 86 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
