dhc acne spot therapy
Generic: sulfur
Labeler: dhc usa incorporatedDrug Facts
Product Profile
Brand Name
dhc acne spot therapy
Generic Name
sulfur
Labeler
dhc usa incorporated
Dosage Form
CREAM
Routes
Active Ingredients
sulfur 6 mg/.2g
Manufacturer
Identifiers & Regulatory
Product NDC
63433-389
Product ID
63433-389_4ae85fb3-936c-45b4-95d9-b3206952cd94
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M006
Listing Expiration
2027-12-31
Marketing Start
2018-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63433389
Hyphenated Format
63433-389
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
dhc acne spot therapy (source: ndc)
Generic Name
sulfur (source: ndc)
Application Number
M006 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 6 mg/.2g
Packaging
- 15 g in 1 TUBE (63433-389-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4ae85fb3-936c-45b4-95d9-b3206952cd94", "openfda": {"unii": ["70FD1KFU70"], "rxcui": ["199632"], "spl_set_id": ["84d49048-95cf-4f14-9698-c746237fec9d"], "manufacturer_name": ["DHC USA Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 g in 1 TUBE (63433-389-00)", "package_ndc": "63433-389-00", "marketing_start_date": "20180101"}], "brand_name": "DHC Acne Spot Therapy", "product_id": "63433-389_4ae85fb3-936c-45b4-95d9-b3206952cd94", "dosage_form": "CREAM", "product_ndc": "63433-389", "generic_name": "Sulfur", "labeler_name": "DHC USA Incorporated", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DHC Acne Spot Therapy", "active_ingredients": [{"name": "SULFUR", "strength": "6 mg/.2g"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180101", "listing_expiration_date": "20271231"}