| Product NDC: | 62750-035 |
| Proprietary Name: | Zicam |
| Non Proprietary Name: | zinc acetate and zinc gluconate |
| Active Ingredient(s): | 2; 1 [hp_X]/1; [hp_X]/1 & nbsp; zinc acetate and zinc gluconate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62750-035 |
| Labeler Name: | Matrixx Initiatives, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20081107 |
| Package NDC: | 62750-035-10 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (62750-035-10) > 25 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC |
| NDC Code | 62750-035-10 |
| Proprietary Name | Zicam |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (62750-035-10) > 25 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC |
| Product NDC | 62750-035 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | zinc acetate and zinc gluconate |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20081107 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Matrixx Initiatives, Inc. |
| Substance Name | ZINC ACETATE; ZINC GLUCONATE |
| Strength Number | 2; 1 |
| Strength Unit | [hp_X]/1; [hp_X]/1 |
| Pharmaceutical Classes |