Package 84289-119-20

Brand: proski zinco skin protectant

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 84289-119-20
Digits Only 8428911920
Product NDC 84289-119
Description

1 TUBE in 1 CARTON (84289-119-20) / 28.4 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2025-04-01
Brand proski zinco skin protectant
Generic zinc oxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "30a68165-7884-3eca-e063-6394a90a8d86", "openfda": {"unii": ["SOI2LOH54Z"], "rxcui": ["198911"], "spl_set_id": ["2cb7f314-beb4-e57f-e063-6394a90ad3ef"], "manufacturer_name": ["PHARMAMED USA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (84289-119-20)  / 28.4 g in 1 TUBE", "package_ndc": "84289-119-20", "marketing_start_date": "20250401"}], "brand_name": "PROSKI ZINCO SKIN PROTECTANT", "product_id": "84289-119_30a68165-7884-3eca-e063-6394a90a8d86", "dosage_form": "OINTMENT", "product_ndc": "84289-119", "generic_name": "ZINC OXIDE", "labeler_name": "PHARMAMED USA INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PROSKI ZINCO SKIN PROTECTANT", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "200 mg/g"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250401", "listing_expiration_date": "20261231"}