United States · FDA National Drug Code directory

Hekla lava

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
0220-2395_f2f38dd9-20d3-8a84-e053-2a95a90a7ed2
Product NDC
0220-2395
Form
PELLET
Composition / generic term
HEKLA LAVA
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
19830303
Source listing expiry
20261231

Source-listed ingredients

  • HEKLA LAVA — 200 [kp_C]/200[kp_C]

These values do not establish equivalence or a dose recommendation.

Packages

  • 200 [kp_C] in 1 TUBE (0220-2395-41) · 0220-2395-41

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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