Package 85439-0102-1

Brand: sulfur spot treatment

Generic: sulfur acne treatment
NDC Package

Package Facts

Identity

Package NDC 85439-0102-1
Digits Only 8543901021
Product NDC 85439-0102
Product ID 85439-0102_31e527e0-ce38-e920-e063-6394a90ac827
Description

15 mL in 1 TUBE (85439-0102-1)

Marketing

Marketing Status
Marketed Since 2025-04-15
Brand sulfur spot treatment
Generic sulfur acne treatment
Sample Package No

Linked Drug Pages (1)

Sulfur Spot Treatment ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "31e527e0-ce38-e920-e063-6394a90ac827", "openfda": {"upc": ["0850070734028"], "unii": ["70FD1KFU70"], "rxcui": ["315220"], "spl_set_id": ["31e527e0-ce37-e920-e063-6394a90ac827"], "manufacturer_name": ["Banuskin, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 mL in 1 TUBE (85439-0102-1)", "package_ndc": "85439-0102-1", "marketing_start_date": "20250415"}], "brand_name": "Sulfur Spot Treatment", "product_id": "85439-0102_31e527e0-ce38-e920-e063-6394a90ac827", "dosage_form": "CREAM", "product_ndc": "85439-0102", "generic_name": "Sulfur Acne Treatment", "labeler_name": "Banuskin, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sulfur Spot Treatment", "active_ingredients": [{"name": "SULFUR", "strength": "10 g/100mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250415", "listing_expiration_date": "20261231"}