belli acne control spot treatment
Generic: sulfur
Labeler: body halo llcDrug Facts
Product Profile
Brand Name
belli acne control spot treatment
Generic Name
sulfur
Labeler
body halo llc
Dosage Form
CREAM
Routes
Active Ingredients
sulfur 30 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
42281-001
Product ID
42281-001_2cdcb7de-ce78-3d94-e063-6394a90a8bec
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M006
Listing Expiration
2026-12-31
Marketing Start
2012-01-02
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42281001
Hyphenated Format
42281-001
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
belli acne control spot treatment (source: ndc)
Generic Name
sulfur (source: ndc)
Application Number
M006 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/mL
Packaging
- 1 TUBE in 1 CARTON (42281-001-00) / 14.75 mL in 1 TUBE
Packages (1)
Ingredients (1)
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"}