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Folli Pilose
Folli Pilose - 52797-030-01 - (WITCH HAZEL)
Drug Information of Folli Pilose
| Product NDC: | 52797-030 |
| Proprietary Name: | Folli Pilose |
| Non Proprietary Name: | WITCH HAZEL |
| Active Ingredient(s): | .15 mL/150mL & nbsp; WITCH HAZEL |
| Administration Route(s): | CUTANEOUS |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Folli Pilose
| Product NDC: | 52797-030 |
| Labeler Name: | MEDIWAY KOREA CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100901 |
Package Information of Folli Pilose
| Package NDC: | 52797-030-01 |
| Package Description: | 150 mL in 1 CARTON (52797-030-01) |
NDC Information of Folli Pilose
| NDC Code | 52797-030-01 |
| Proprietary Name | Folli Pilose |
| Package Description | 150 mL in 1 CARTON (52797-030-01) |
| Product NDC | 52797-030 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | WITCH HAZEL |
| Dosage Form Name | SPRAY |
| Route Name | CUTANEOUS |
| Start Marketing Date | 20100901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | MEDIWAY KOREA CO., LTD. |
| Substance Name | WITCH HAZEL |
| Strength Number | .15 |
| Strength Unit | mL/150mL |
| Pharmaceutical Classes |
