United States · FDA National Drug Code directory

OXALICUM ACIDUM

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
0220-3838_3a9d4e84-118f-0eca-e063-6294a90a73cc
Product NDC
0220-3838
Form
PELLET
Composition / generic term
OXALIC ACID DIHYDRATE
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20250101
Source listing expiry
20261231

Source-listed ingredients

  • OXALIC ACID DIHYDRATE — 200 [kp_C]/200[kp_C]

These values do not establish equivalence or a dose recommendation.

Packages

  • 200 [kp_C] in 1 TUBE (0220-3838-41) · 0220-3838-41

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.

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OXALICUM ACIDUM — United States | Molindra Medicines