United States · FDA National Drug Code directory

D-112

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
58264-0118_2b9eda10-4e9d-e31e-e063-6394a90a53c6
Product NDC
58264-0118
Form
SOLUTION
Composition / generic term
Lachesis Muta venom, Silicon dioxide, Sodium chloride, Ranunculus bulbosus, Aconitum napellus, Activated charcoal, Nitroglycerin, Oyster shell calcium carbonate, crude, Anemone pratensis, Plantago major, arsenic trioxide, and Magnesium phosphate, dibasic trihydrate
Labeler
DNA Labs, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
19900101
Source listing expiry
20261231

Source-listed ingredients

  • LACHESIS MUTA VENOM — 12 [hp_X]/mL
  • SILICON DIOXIDE — 8 [hp_X]/mL
  • SODIUM CHLORIDE — 4 [hp_X]/mL
  • RANUNCULUS BULBOSUS — 4 [hp_X]/mL
  • ACONITUM NAPELLUS — 4 [hp_X]/mL
  • ACTIVATED CHARCOAL — 8 [hp_X]/mL
  • NITROGLYCERIN — 6 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE — 8 [hp_X]/mL
  • ANEMONE PRATENSIS — 4 [hp_X]/mL
  • PLANTAGO MAJOR — 4 [hp_X]/mL
  • ARSENIC TRIOXIDE — 6 [hp_X]/mL
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE — 4 [hp_X]/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 29.57 mL in 1 BOTTLE, GLASS (58264-0118-1) · 58264-0118-1

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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