United States · FDA National Drug Code directory
D-59
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
- 58264-0059_2b9ed194-deed-363e-e063-6294a90a8cdc
- Product NDC
- 58264-0059
- Form
- SOLUTION
- Composition / generic term
- Fucus vesiculosus, Spongia officinalis skeleton, roasted, Graphite, Oyster shell calcium carbonate, crude, Sodium sulfate, and Croton oil
- Labeler
- DNA Labs, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 19900101
- Source listing expiry
- 20261231
Source-listed ingredients
- FUCUS VESICULOSUS — 3 [hp_X]/mL
- SPONGIA OFFICINALIS SKELETON, ROASTED — 3 [hp_X]/mL
- GRAPHITE — 12 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE — 12 [hp_X]/mL
- SODIUM SULFATE — 2 [hp_X]/mL
- CROTON OIL — 4 [hp_X]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 29.57 mL in 1 BOTTLE, GLASS (58264-0059-1) · 58264-0059-1
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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