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 |