borax
Generic: borax
Labeler: ohm pharma inc.Drug Facts
Product Profile
Brand Name
borax
Generic Name
borax
Labeler
ohm pharma inc.
Dosage Form
PELLET
Routes
Active Ingredients
sodium borate 6 [hp_C]/6[hp_C]
Manufacturer
Identifiers & Regulatory
Product NDC
66096-800
Product ID
66096-800_d450f5ab-364d-46cd-e053-2995a90addd1
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
2019-11-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
66096800
Hyphenated Format
66096-800
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
borax (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 6 [hp_C]/6[hp_C]
Packaging
- 6 [hp_C] in 1 TUBE (66096-800-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d450f5ab-364d-46cd-e053-2995a90addd1", "openfda": {"unii": ["91MBZ8H3QO"], "spl_set_id": ["2d5f7e06-1195-4ff9-a1e6-cf64c4f7cc4d"], "manufacturer_name": ["OHM PHARMA INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (66096-800-01)", "package_ndc": "66096-800-01", "marketing_start_date": "20191101"}], "brand_name": "Borax", "product_id": "66096-800_d450f5ab-364d-46cd-e053-2995a90addd1", "dosage_form": "PELLET", "product_ndc": "66096-800", "generic_name": "BORAX", "labeler_name": "OHM PHARMA INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Borax", "active_ingredients": [{"name": "SODIUM BORATE", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20191101", "listing_expiration_date": "20261231"}