spot defy
Generic: sulfur
Labeler: bioelements, inc.Drug Facts
Product Profile
Brand Name
spot defy
Generic Name
sulfur
Labeler
bioelements, inc.
Dosage Form
LOTION
Routes
Active Ingredients
sulfur 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
49825-200
Product ID
49825-200_462acf75-cc59-2738-e063-6294a90a47de
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M006
Listing Expiration
2027-12-31
Marketing Start
2024-09-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
49825200
Hyphenated Format
49825-200
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
spot defy (source: ndc)
Generic Name
sulfur (source: ndc)
Application Number
M006 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/mL
Packaging
- 1 BOTTLE, GLASS in 1 CARTON (49825-200-10) / 15 mL in 1 BOTTLE, GLASS (49825-200-20)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "462acf75-cc59-2738-e063-6294a90a47de", "openfda": {"unii": ["70FD1KFU70"], "rxcui": ["422938"], "spl_set_id": ["6f35f950-8d04-4181-a897-5679fde1e2d9"], "manufacturer_name": ["Bioelements, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, GLASS in 1 CARTON (49825-200-10) / 15 mL in 1 BOTTLE, GLASS (49825-200-20)", "package_ndc": "49825-200-10", "marketing_start_date": "20240901"}], "brand_name": "Spot Defy", "product_id": "49825-200_462acf75-cc59-2738-e063-6294a90a47de", "dosage_form": "LOTION", "product_ndc": "49825-200", "generic_name": "Sulfur", "labeler_name": "Bioelements, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Spot Defy", "active_ingredients": [{"name": "SULFUR", "strength": "50 mg/mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240901", "listing_expiration_date": "20271231"}