Package 82442-384-01

Brand: up and up medicated anti-dandruff anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis

Generic: selenium sulfide
NDC Package

Package Facts

Identity

Package NDC 82442-384-01
Digits Only 8244238401
Product NDC 82442-384
Description

355 mL in 1 BOTTLE (82442-384-01)

Marketing

Marketing Status
Marketed Since 2024-04-04
Brand up and up medicated anti-dandruff anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis
Generic selenium sulfide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "f1856542-23c1-48ca-921a-62d9b42ac5a8", "openfda": {"unii": ["Z69D9E381Q"], "rxcui": ["204642"], "spl_set_id": ["a516282f-ed6b-4e94-b269-ea34f700dd69"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (82442-384-01)", "package_ndc": "82442-384-01", "marketing_start_date": "20240404"}], "brand_name": "up and up Medicated Anti-dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis", "product_id": "82442-384_f1856542-23c1-48ca-921a-62d9b42ac5a8", "dosage_form": "SHAMPOO", "product_ndc": "82442-384", "generic_name": "SELENIUM SULFIDE", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up Medicated Anti-dandruff", "brand_name_suffix": "Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis", "active_ingredients": [{"name": "SELENIUM SULFIDE", "strength": "10 mg/mL"}], "application_number": "M032", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240404", "listing_expiration_date": "20261231"}