sulphur
Generic: sulphur
Labeler: energique, inc.Drug Facts
Product Profile
Brand Name
sulphur
Generic Name
sulphur
Labeler
energique, inc.
Dosage Form
LIQUID
Routes
Active Ingredients
sulfur 200 [hp_C]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
44911-0394
Product ID
44911-0394_5add97fb-ea3c-44b3-b068-3a5136924449
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
2016-08-23
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
449110394
Hyphenated Format
44911-0394
Supplemental Identifiers
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
sulphur (source: ndc)
Generic Name
sulphur (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 [hp_C]/mL
Packaging
- 30 mL in 1 BOTTLE, DROPPER (44911-0394-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5add97fb-ea3c-44b3-b068-3a5136924449", "openfda": {"unii": ["70FD1KFU70"], "spl_set_id": ["4c194575-9ac3-436a-9b49-f228146a0bda"], "manufacturer_name": ["Energique, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE, DROPPER (44911-0394-1)", "package_ndc": "44911-0394-1", "marketing_start_date": "20160823"}], "brand_name": "Sulphur", "product_id": "44911-0394_5add97fb-ea3c-44b3-b068-3a5136924449", "dosage_form": "LIQUID", "product_ndc": "44911-0394", "generic_name": "Sulphur", "labeler_name": "Energique, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sulphur", "active_ingredients": [{"name": "SULFUR", "strength": "200 [hp_C]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20160823", "listing_expiration_date": "20261231"}