Package 70000-0748-1

Brand: dandruff

Generic: pyrithione zinc
NDC Package

Package Facts

Identity

Package NDC 70000-0748-1
Digits Only 7000007481
Product NDC 70000-0748
Description

369 mL in 1 BOTTLE, PLASTIC (70000-0748-1)

Marketing

Marketing Status
Marketed Since 2025-11-07
Brand dandruff
Generic pyrithione zinc
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3dc8a55c-2d58-4ff5-bf7d-65bc6a8b8033", "openfda": {"unii": ["R953O2RHZ5"], "rxcui": ["209884"], "spl_set_id": ["d85f9017-6ab5-4ad6-a7f0-5570b20093cb"], "manufacturer_name": ["CARDINAL HEALTH 110, LLC. DBA LEADER"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "369 mL in 1 BOTTLE, PLASTIC (70000-0748-1)", "package_ndc": "70000-0748-1", "marketing_start_date": "20251107"}], "brand_name": "Dandruff", "product_id": "70000-0748_3dc8a55c-2d58-4ff5-bf7d-65bc6a8b8033", "dosage_form": "SHAMPOO", "product_ndc": "70000-0748", "generic_name": "Pyrithione Zinc", "labeler_name": "CARDINAL HEALTH 110, LLC. DBA LEADER", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dandruff", "active_ingredients": [{"name": "PYRITHIONE ZINC", "strength": "10 mg/mL"}], "application_number": "M032", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191010", "listing_expiration_date": "20261231"}