borax
Generic: sodium borate
Labeler: boironDrug Facts
Product Profile
Brand Name
borax
Generic Name
sodium borate
Labeler
boiron
Dosage Form
PELLET
Routes
Active Ingredients
sodium borate 6 [hp_X]/1
Manufacturer
Identifiers & Regulatory
Product NDC
0220-0887
Product ID
0220-0887_04115ec1-ef2d-1746-e063-6394a90a0a52
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
1983-03-03
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02200887
Hyphenated Format
0220-0887
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
borax (source: ndc)
Generic Name
sodium borate (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 6 [hp_X]/1
Packaging
- 80 PELLET in 1 TUBE (0220-0887-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "04115ec1-ef2d-1746-e063-6394a90a0a52", "openfda": {"unii": ["91MBZ8H3QO"], "spl_set_id": ["b183d580-79fe-11e6-b18d-424c58303031"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 PELLET in 1 TUBE (0220-0887-41)", "package_ndc": "0220-0887-41", "marketing_start_date": "19830303"}], "brand_name": "Borax", "product_id": "0220-0887_04115ec1-ef2d-1746-e063-6394a90a0a52", "dosage_form": "PELLET", "product_ndc": "0220-0887", "generic_name": "SODIUM BORATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Borax", "active_ingredients": [{"name": "SODIUM BORATE", "strength": "6 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}