Package 70707-440-04

Brand: sulfur spot treatment

Generic: sulfur
NDC Package

Package Facts

Identity

Package NDC 70707-440-04
Digits Only 7070744004
Product NDC 70707-440
Description

118 mL in 1 BOTTLE (70707-440-04)

Marketing

Marketing Status
Marketed Since 2020-01-15
Brand sulfur spot treatment
Generic sulfur
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "28da58df-4226-e6db-e063-6394a90aced8", "openfda": {"upc": ["0812223030111"], "unii": ["70FD1KFU70"], "rxcui": ["2273805"], "spl_set_id": ["921e948d-a8c7-4527-9257-4b91dee8fcff"], "manufacturer_name": ["Face Reality, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE (70707-440-04)", "package_ndc": "70707-440-04", "marketing_start_date": "20200115"}, {"sample": false, "description": "1 TUBE in 1 BOX (70707-440-15)  / 44 mL in 1 TUBE", "package_ndc": "70707-440-15", "marketing_start_date": "20200108"}], "brand_name": "Sulfur Spot Treatment", "product_id": "70707-440_28da58df-4226-e6db-e063-6394a90aced8", "dosage_form": "GEL", "product_ndc": "70707-440", "generic_name": "SULFUR", "labeler_name": "Face Reality, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sulfur Spot Treatment", "active_ingredients": [{"name": "SULFUR", "strength": "60 mg/mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200108", "listing_expiration_date": "20261231"}