d-103
Generic: aluminum oxide, silver, gold, beryllium, cadmium, copper, calcium sulfide, mercuric sulfate, molybdenum, nickel, plantago major, platinum, lead, anemone pratensis, selenium, and tin
Labeler: dna labs, inc.Drug Facts
Product Profile
Brand Name
d-103
Generic Name
aluminum oxide, silver, gold, beryllium, cadmium, copper, calcium sulfide, mercuric sulfate, molybdenum, nickel, plantago major, platinum, lead, anemone pratensis, selenium, and tin
Labeler
dna labs, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
aluminum oxide 30 [hp_X]/mL, anemone pratensis 6 [hp_X]/mL, beryllium 30 [hp_X]/mL, cadmium 30 [hp_X]/mL, calcium sulfide 12 [hp_X]/mL, copper 30 [hp_X]/mL, gold 30 [hp_X]/mL, lead 30 [hp_X]/mL, mercuric sulfate 30 [hp_X]/mL, molybdenum 30 [hp_X]/mL, nickel 30 [hp_X]/mL, plantago major 4 [hp_X]/mL, platinum 30 [hp_X]/mL, selenium 30 [hp_X]/mL, silver 30 [hp_X]/mL, tin 30 [hp_X]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
58264-0109
Product ID
58264-0109_2b9ecbda-710d-d64a-e063-6294a90aac9e
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
1990-01-01
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
582640109
Hyphenated Format
58264-0109
Supplemental Identifiers
UNII
NUI
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
d-103 (source: ndc)
Generic Name
aluminum oxide, silver, gold, beryllium, cadmium, copper, calcium sulfide, mercuric sulfate, molybdenum, nickel, plantago major, platinum, lead, anemone pratensis, selenium, and tin (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 [hp_X]/mL
- 6 [hp_X]/mL
- 12 [hp_X]/mL
- 4 [hp_X]/mL
Packaging
- 29.57 mL in 1 BOTTLE, GLASS (58264-0109-1)
Packages (1)
Ingredients (16)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["SUBLINGUAL"], "spl_id": "2b9ecbda-710d-d64a-e063-6294a90aac9e", "openfda": {"nui": ["M0005152", "N0000175831", "N0000008595", "N0000008924", "N0000175830", "N0000185508", "N0000175629", "N0000184306", "M0000728"], "unii": ["LMI26O6933", "8E272251DI", "OW5102UV6N", "00BH33GNGH", "1MBW07J51Q", "789U1901C5", "79Y1949PYO", "2P299V784P", "J4L3PPG58I", "81AH48963U", "7OV03QG267", "W2469WNO6U", "49DFR088MY", "H6241UJ22B", "3M4G523W1G", "387GMG9FH5"], "spl_set_id": ["f4efd03d-3f80-4694-9a02-b71b7e3e3f0d"], "pharm_class_cs": ["Copper [CS]", "Allergens [CS]"], "pharm_class_pe": ["Decreased Embryonic Implantation [PE]", "Decreased Sperm Motility [PE]", "Inhibit Ovum Fertilization [PE]", "Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]"], "pharm_class_epc": ["Copper-containing Intrauterine Device [EPC]", "Standardized Chemical Allergen [EPC]"], "manufacturer_name": ["DNA Labs, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "29.57 mL in 1 BOTTLE, GLASS (58264-0109-1)", "package_ndc": "58264-0109-1", "marketing_start_date": "19900101"}], "brand_name": "D-103", "product_id": "58264-0109_2b9ecbda-710d-d64a-e063-6294a90aac9e", "dosage_form": "SOLUTION", "pharm_class": ["Allergens [CS]", "Allergens [CS]", "Cell-mediated Immunity [PE]", "Cell-mediated Immunity [PE]", "Copper [CS]", "Copper-containing Intrauterine Device [EPC]", "Decreased Embryonic Implantation [PE]", "Decreased Sperm Motility [PE]", "Increased Histamine Release [PE]", "Increased Histamine Release [PE]", "Increased Large Intestinal Motility [PE]", "Inhibit Ovum Fertilization [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Standardized Chemical Allergen [EPC]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "58264-0109", "generic_name": "Aluminum oxide, Silver, Gold, Beryllium, Cadmium, Copper, Calcium sulfide, Mercuric sulfate, Molybdenum, Nickel, Plantago major, Platinum, Lead, Anemone pratensis, Selenium, and Tin", "labeler_name": "DNA Labs, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "D-103", "active_ingredients": [{"name": "ALUMINUM OXIDE", "strength": "30 [hp_X]/mL"}, {"name": "ANEMONE PRATENSIS", "strength": "6 [hp_X]/mL"}, {"name": "BERYLLIUM", "strength": "30 [hp_X]/mL"}, {"name": "CADMIUM", "strength": "30 [hp_X]/mL"}, {"name": "CALCIUM SULFIDE", "strength": "12 [hp_X]/mL"}, {"name": "COPPER", "strength": "30 [hp_X]/mL"}, {"name": "GOLD", "strength": "30 [hp_X]/mL"}, {"name": "LEAD", "strength": "30 [hp_X]/mL"}, {"name": "MERCURIC SULFATE", "strength": "30 [hp_X]/mL"}, {"name": "MOLYBDENUM", "strength": "30 [hp_X]/mL"}, {"name": "NICKEL", "strength": "30 [hp_X]/mL"}, {"name": "PLANTAGO MAJOR", "strength": "4 [hp_X]/mL"}, {"name": "PLATINUM", "strength": "30 [hp_X]/mL"}, {"name": "SELENIUM", "strength": "30 [hp_X]/mL"}, {"name": "SILVER", "strength": "30 [hp_X]/mL"}, {"name": "TIN", "strength": "30 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19900101", "listing_expiration_date": "20261231"}