| Product NDC: | 43074-207 |
| Proprietary Name: | VenomX |
| Non Proprietary Name: | zinc acetate |
| Active Ingredient(s): | .001 mg/mL & nbsp; zinc acetate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 43074-207 |
| Labeler Name: | Phillips Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100823 |
| Package NDC: | 43074-207-02 |
| Package Description: | 1 BOTTLE, DROPPER in 1 BOTTLE, PLASTIC (43074-207-02) > 3 mL in 1 BOTTLE, DROPPER (43074-207-01) |
| NDC Code | 43074-207-02 |
| Proprietary Name | VenomX |
| Package Description | 1 BOTTLE, DROPPER in 1 BOTTLE, PLASTIC (43074-207-02) > 3 mL in 1 BOTTLE, DROPPER (43074-207-01) |
| Product NDC | 43074-207 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | zinc acetate |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100823 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Phillips Company |
| Substance Name | ZINC ACETATE |
| Strength Number | .001 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |