Package 50804-883-01

Brand: goodsense medicated dandruff anti-seborrheic dermatitis, anti-dandruff

Generic: selenium sulfide
NDC Package

Package Facts

Identity

Package NDC 50804-883-01
Digits Only 5080488301
Product NDC 50804-883
Product ID 50804-883_f5356ff2-25b0-42ab-92de-0cdf350de88d
Description

325 mL in 1 BOTTLE, PLASTIC (50804-883-01)

Marketing

Marketing Status
Marketed Since 2018-03-01
Brand goodsense medicated dandruff anti-seborrheic dermatitis, anti-dandruff
Generic selenium sulfide
Sample Package No

Linked Drug Pages (1)

GoodSense Medicated Dandruff Anti-Seborrheic Dermatitis, Anti-Dandruff ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "f5356ff2-25b0-42ab-92de-0cdf350de88d", "openfda": {"unii": ["Z69D9E381Q"], "rxcui": ["204642"], "spl_set_id": ["21291e29-57ab-4761-8e8c-eef43ca65b24"], "manufacturer_name": ["GOODSENSE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "325 mL in 1 BOTTLE, PLASTIC (50804-883-01)", "package_ndc": "50804-883-01", "marketing_start_date": "20180301"}], "brand_name": "GoodSense Medicated Dandruff Anti-Seborrheic Dermatitis, Anti-Dandruff", "product_id": "50804-883_f5356ff2-25b0-42ab-92de-0cdf350de88d", "dosage_form": "SHAMPOO", "product_ndc": "50804-883", "generic_name": "Selenium Sulfide", "labeler_name": "GOODSENSE", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GoodSense Medicated Dandruff", "brand_name_suffix": "Anti-Seborrheic Dermatitis, Anti-Dandruff", "active_ingredients": [{"name": "SELENIUM SULFIDE", "strength": "10 mg/mL"}], "application_number": "M032", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180301", "listing_expiration_date": "20261231"}