United States · FDA National Drug Code directory

Arniflora Gel

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
68466-0004_11f1a77b-71cd-41fb-945f-6d7d1d9b12e2
Product NDC
68466-0004
Form
GEL
Composition / generic term
ARNICA MONTANA
Labeler
Schwabe Mexico S.A. de C.V.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20110101
Source listing expiry
20261231

Source-listed ingredients

  • ARNICA MONTANA — 1 [hp_X]/28g

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 TUBE in 1 CARTON (68466-0004-8) / 78 g in 1 TUBE · 68466-0004-8

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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