United States · FDA National Drug Code directory

D-33

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
58264-0033_2b9eb825-2e83-846c-e063-6394a90a0a7b
Product NDC
58264-0033
Form
SOLUTION
Composition / generic term
ATROPA BELLADONNA, BUFO BUFO CUTANEOUS GLAND, COPPER, ANEMONE PRATENSIS, SILICON DIOXIDE, and ZINC
Labeler
DNA Labs, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
19900101
Source listing expiry
20261231

Source-listed ingredients

  • ATROPA BELLADONNA — 30 [hp_X]/mL
  • BUFO BUFO CUTANEOUS GLAND — 200 [hp_X]/mL
  • COPPER — 12 [hp_X]/mL
  • ANEMONE PRATENSIS — 30 [hp_X]/mL
  • SILICON DIOXIDE — 30 [hp_X]/mL
  • ZINC — 12 [hp_X]/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 29.57 mL in 1 BOTTLE, GLASS (58264-0033-1) · 58264-0033-1

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →