United States · FDA National Drug Code directory

N-13

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: 58264-0211_2b538be3-baa8-3c2b-e063-6294a90a1489
Product NDC: 58264-0211
Form: SOLUTION
Composition / generic term: Ceanothus americanus leaf, Urtica urens, Sodium Chloride, Lachesis muta whole, Cinchona officinalis Bark, Lycopodium clavatum Whole, Ferric chloride hexahydrate, and Sus scrofa spleen
Labeler: DNA Labs, Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start / end (source format): 19900101
Source listing expiry: 20261231

Source-listed ingredients

CEANOTHUS AMERICANUS LEAF — 4 [hp_X]/mL
URTICA URENS — 4 [hp_X]/mL
SODIUM CHLORIDE — 6 [hp_X]/mL
LACHESIS MUTA WHOLE — 12 [hp_X]/mL
CINCHONA OFFICINALIS BARK — 8 [hp_X]/mL
LYCOPODIUM CLAVATUM WHOLE — 6 [hp_X]/mL
FERRIC CHLORIDE HEXAHYDRATE — 6 [hp_X]/mL
SUS SCROFA SPLEEN — 200 [hp_X]/mL

These values do not establish equivalence or a dose recommendation.

Packages

29.57 mL in 1 BOTTLE, GLASS (58264-0211-1) · 58264-0211-1

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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