Package 84697-001-01

Brand: zeus

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 84697-001-01
Digits Only 8469700101
Product NDC 84697-001
Description

1 BOTTLE in 1 CARTON (84697-001-01) / 50 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-09-26
Brand zeus
Generic zinc oxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "436d9732-c5cf-9e81-e063-6394a90a902c", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["5354c383-08f0-4b89-b36a-96a35f47be3c"], "manufacturer_name": ["NEWPORT APOTHECARY, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (84697-001-01)  / 50 mL in 1 BOTTLE", "package_ndc": "84697-001-01", "marketing_start_date": "20240926"}], "brand_name": "ZEUS", "product_id": "84697-001_436d9732-c5cf-9e81-e063-6394a90a902c", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "84697-001", "generic_name": "ZINC OXIDE", "labeler_name": "NEWPORT APOTHECARY, INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ZEUS", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "22.3 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240926", "listing_expiration_date": "20261231"}