Package 0220-5486-41

Brand: zincum sulphuricum

Generic: zinc sulfate heptahydrate
NDC Package

Package Facts

Identity

Package NDC 0220-5486-41
Digits Only 0220548641
Product NDC 0220-5486
Description

200 [kp_C] in 1 TUBE (0220-5486-41)

Marketing

Marketing Status
Marketed Since 2024-01-01
Brand zincum sulphuricum
Generic zinc sulfate heptahydrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "21b581c7-06e9-dea3-e063-6294a90a91a3", "openfda": {"unii": ["N57JI2K7WP"], "spl_set_id": ["21b581c7-06e8-dea3-e063-6294a90a91a3"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-5486-41)", "package_ndc": "0220-5486-41", "marketing_start_date": "20240101"}], "brand_name": "Zincum sulphuricum", "product_id": "0220-5486_21b581c7-06e9-dea3-e063-6294a90a91a3", "dosage_form": "PELLET", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "0220-5486", "generic_name": "ZINC SULFATE HEPTAHYDRATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Zincum sulphuricum", "active_ingredients": [{"name": "ZINC SULFATE HEPTAHYDRATE", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}