natrum sulph
Generic: natrum sulph
Labeler: rxhomeo private limited d.b.a. rxhomeo, incDrug Facts
Product Profile
Brand Name
natrum sulph
Generic Name
natrum sulph
Labeler
rxhomeo private limited d.b.a. rxhomeo, inc
Dosage Form
LIQUID
Routes
Active Ingredients
sodium sulfate 1 [hp_X]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
15631-2863
Product ID
15631-2863_1a229f59-cf27-3267-e063-6394a90a6424
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
2024-05-23
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
156312863
Hyphenated Format
15631-2863
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
natrum sulph (source: ndc)
Generic Name
natrum sulph (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 [hp_X]/mL
Packaging
- 10 mL in 1 BOTTLE (15631-2863-0)
- 30 mL in 1 BOTTLE (15631-2863-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1a229f59-cf27-3267-e063-6394a90a6424", "openfda": {"unii": ["0YPR65R21J"], "spl_set_id": ["1a229b91-7cc7-3442-e063-6394a90a6692"], "manufacturer_name": ["Rxhomeo Private Limited d.b.a. Rxhomeo, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 BOTTLE (15631-2863-0)", "package_ndc": "15631-2863-0", "marketing_start_date": "20240523"}, {"sample": false, "description": "30 mL in 1 BOTTLE (15631-2863-1)", "package_ndc": "15631-2863-1", "marketing_start_date": "20240523"}], "brand_name": "NATRUM SULPH", "product_id": "15631-2863_1a229f59-cf27-3267-e063-6394a90a6424", "dosage_form": "LIQUID", "product_ndc": "15631-2863", "generic_name": "NATRUM SULPH", "labeler_name": "Rxhomeo Private Limited d.b.a. Rxhomeo, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NATRUM SULPH", "active_ingredients": [{"name": "SODIUM SULFATE", "strength": "1 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240523", "listing_expiration_date": "20261231"}