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Snowberry
Snowberry - 58231-001-01 - (Zinc Oxide)
Drug Information of Snowberry
| Product NDC: | 58231-001 |
| Proprietary Name: | Snowberry |
| Non Proprietary Name: | Zinc Oxide |
| Active Ingredient(s): | .7; .7; .3; 1.6 g/10g; g/10g; g/10g; g/10g & nbsp; Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Snowberry
| Product NDC: | 58231-001 |
| Labeler Name: | Snowberry New Zealand Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130401 |
Package Information of Snowberry
| Package NDC: | 58231-001-01 |
| Package Description: | 1 TUBE in 1 CARTON (58231-001-01) > 50 g in 1 TUBE |
NDC Information of Snowberry
| NDC Code | 58231-001-01 |
| Proprietary Name | Snowberry |
| Package Description | 1 TUBE in 1 CARTON (58231-001-01) > 50 g in 1 TUBE |
| Product NDC | 58231-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130401 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Snowberry New Zealand Ltd |
| Substance Name | ETHYL FERULATE; KAEMPFERIA GALANGA ROOT; LARIX SIBIRICA WOOD; ZINC OXIDE |
| Strength Number | .7; .7; .3; 1.6 |
| Strength Unit | g/10g; g/10g; g/10g; g/10g |
| Pharmaceutical Classes |
