Package 42281-001-00

Brand: belli acne control spot treatment

Generic: sulfur
NDC Package

Package Facts

Identity

Package NDC 42281-001-00
Digits Only 4228100100
Product NDC 42281-001
Description

1 TUBE in 1 CARTON (42281-001-00) / 14.75 mL in 1 TUBE

Marketing

Marketing Status
Marketed Since 2022-02-01
Brand belli acne control 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": "2cdcb7de-ce78-3d94-e063-6394a90a8bec", "openfda": {"unii": ["70FD1KFU70"], "rxcui": ["199632"], "spl_set_id": ["da979b69-1e4c-4e2b-82c3-0f155e978652"], "manufacturer_name": ["BODY HALO LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (42281-001-00)  / 14.75 mL in 1 TUBE", "package_ndc": "42281-001-00", "marketing_start_date": "20220201"}], "brand_name": "Belli Acne Control Spot Treatment", "product_id": "42281-001_2cdcb7de-ce78-3d94-e063-6394a90a8bec", "dosage_form": "CREAM", "product_ndc": "42281-001", "generic_name": "SULFUR", "labeler_name": "BODY HALO LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Belli Acne Control Spot Treatment", "active_ingredients": [{"name": "SULFUR", "strength": "30 mg/mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20120102", "listing_expiration_date": "20261231"}