d-120

Generic: calcium fluoride, bismuth subnitrate, zinc, mercuric chloride, toxicodendron pubescens leaf, antimony trisulfide, barium carbonate, echinacea angustifolia, iodine, phosphoric acid, potassium carbonate, dibasic potassium phosphate, and thuja occidentalis leafy twig

Labeler: dna labs, inc.
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name d-120
Generic Name calcium fluoride, bismuth subnitrate, zinc, mercuric chloride, toxicodendron pubescens leaf, antimony trisulfide, barium carbonate, echinacea angustifolia, iodine, phosphoric acid, potassium carbonate, dibasic potassium phosphate, and thuja occidentalis leafy twig
Labeler dna labs, inc.
Dosage Form SOLUTION
Routes
SUBLINGUAL
Active Ingredients

antimony trisulfide 8 [hp_X]/mL, barium carbonate 8 [hp_X]/mL, bismuth subnitrate 6 [hp_X]/mL, calcium fluoride 8 [hp_X]/mL, dibasic potassium phosphate 4 [hp_X]/mL, echinacea angustifolia 4 [hp_X]/mL, iodine 4 [hp_X]/mL, mercuric chloride 6 [hp_X]/mL, phosphoric acid 4 [hp_X]/mL, potassium carbonate 6 [hp_X]/mL, thuja occidentalis leafy twig 4 [hp_X]/mL, toxicodendron pubescens leaf 4 [hp_X]/mL, zinc 8 [hp_X]/mL

Manufacturer
DNA Labs, Inc.

Identifiers & Regulatory

Product NDC 58264-0126
Product ID 58264-0126_2b9ef26a-132d-fdee-e063-6394a90abb13
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 1990-01-01

Pharmacologic Class

Classes
bismuth [cs] bismuth [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 582640126
Hyphenated Format 58264-0126

Supplemental Identifiers

UNII
F79059A38U 6P669D8HQ8 H19J064BA5 O3B55K4YKI CI71S98N1Z VB06AV5US8 9679TC07X4 53GH7MZT1R E4GA8884NN BQN1B9B9HA 1NT28V9397 6IO182RP7A J41CSQ7QDS

Packaging Origin

Original Packager
true

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 d-120 (source: ndc)
Generic Name calcium fluoride, bismuth subnitrate, zinc, mercuric chloride, toxicodendron pubescens leaf, antimony trisulfide, barium carbonate, echinacea angustifolia, iodine, phosphoric acid, potassium carbonate, dibasic potassium phosphate, and thuja occidentalis leafy twig (source: ndc)
Routes
SUBLINGUAL
source: ndc

Resolved Composition

Strengths
  • 8 [hp_X]/mL
  • 6 [hp_X]/mL
  • 4 [hp_X]/mL
source: ndc
Packaging
  • 29.57 mL in 1 BOTTLE, GLASS (58264-0126-1)
source: ndc

Packages (1)

Ingredients (13)

antimony trisulfide (8 [hp_X]/mL) barium carbonate (8 [hp_X]/mL) bismuth subnitrate (6 [hp_X]/mL) calcium fluoride (8 [hp_X]/mL) dibasic potassium phosphate (4 [hp_X]/mL) echinacea angustifolia (4 [hp_X]/mL) iodine (4 [hp_X]/mL) mercuric chloride (6 [hp_X]/mL) phosphoric acid (4 [hp_X]/mL) potassium carbonate (6 [hp_X]/mL) thuja occidentalis leafy twig (4 [hp_X]/mL) toxicodendron pubescens leaf (4 [hp_X]/mL) zinc (8 [hp_X]/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBLINGUAL"], "spl_id": "2b9ef26a-132d-fdee-e063-6394a90abb13", "openfda": {"unii": ["F79059A38U", "6P669D8HQ8", "H19J064BA5", "O3B55K4YKI", "CI71S98N1Z", "VB06AV5US8", "9679TC07X4", "53GH7MZT1R", "E4GA8884NN", "BQN1B9B9HA", "1NT28V9397", "6IO182RP7A", "J41CSQ7QDS"], "spl_set_id": ["9525c016-f0dd-43fd-a4e9-062075107eec"], "manufacturer_name": ["DNA Labs, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "29.57 mL in 1 BOTTLE, GLASS (58264-0126-1)", "package_ndc": "58264-0126-1", "marketing_start_date": "19900101"}], "brand_name": "D-120", "product_id": "58264-0126_2b9ef26a-132d-fdee-e063-6394a90abb13", "dosage_form": "SOLUTION", "pharm_class": ["Bismuth [CS]", "Bismuth [EPC]"], "product_ndc": "58264-0126", "generic_name": "Calcium fluoride, Bismuth Subnitrate, Zinc, Mercuric Chloride, Toxicodendron pubescens leaf, Antimony trisulfide, Barium carbonate, Echinacea angustifolia, Iodine, Phosphoric acid, Potassium carbonate, Dibasic potassium phosphate, and Thuja occidentalis Leafy twig", "labeler_name": "DNA Labs, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "D-120", "active_ingredients": [{"name": "ANTIMONY TRISULFIDE", "strength": "8 [hp_X]/mL"}, {"name": "BARIUM CARBONATE", "strength": "8 [hp_X]/mL"}, {"name": "BISMUTH SUBNITRATE", "strength": "6 [hp_X]/mL"}, {"name": "CALCIUM FLUORIDE", "strength": "8 [hp_X]/mL"}, {"name": "DIBASIC POTASSIUM PHOSPHATE", "strength": "4 [hp_X]/mL"}, {"name": "ECHINACEA ANGUSTIFOLIA", "strength": "4 [hp_X]/mL"}, {"name": "IODINE", "strength": "4 [hp_X]/mL"}, {"name": "MERCURIC CHLORIDE", "strength": "6 [hp_X]/mL"}, {"name": "PHOSPHORIC ACID", "strength": "4 [hp_X]/mL"}, {"name": "POTASSIUM CARBONATE", "strength": "6 [hp_X]/mL"}, {"name": "THUJA OCCIDENTALIS LEAFY TWIG", "strength": "4 [hp_X]/mL"}, {"name": "TOXICODENDRON PUBESCENS LEAF", "strength": "4 [hp_X]/mL"}, {"name": "ZINC", "strength": "8 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19900101", "listing_expiration_date": "20261231"}