sulfur spot treatment

Generic: sulfur acne treatment

Labeler: banuskin, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sulfur spot treatment
Generic Name sulfur acne treatment
Labeler banuskin, inc.
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

sulfur 10 g/100mL

Manufacturer
Banuskin, Inc.

Identifiers & Regulatory

Product NDC 85439-0102
Product ID 85439-0102_31e527e0-ce38-e920-e063-6394a90ac827
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M006
Listing Expiration 2026-12-31
Marketing Start 2025-04-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 854390102
Hyphenated Format 85439-0102

Supplemental Identifiers

RxCUI
315220
UPC
0850070734028
UNII
70FD1KFU70

Packaging Origin

Original Packager
true

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 sulfur spot treatment (source: ndc)
Generic Name sulfur acne treatment (source: ndc)
Application Number M006 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 10 g/100mL
source: ndc
Packaging
  • 15 mL in 1 TUBE (85439-0102-1)
source: ndc

Packages (1)

Ingredients (1)

sulfur (10 g/100mL)

Linked Drug Pages (1)

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"}