United States · FDA National Drug Code directory

Triflora 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: 68466-2001_e3f082b2-ad1c-4ed8-a077-bb2bc4d2134d
Product NDC: 68466-2001
Form: GEL
Composition / generic term: URTICA DIOICA, TOXICODENDRON PUBESCENS LEAF, LEDUM PALUSTRE TWIG
Labeler: Schwabe Mexico S.A. de C.V.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start / end (source format): 20211001
Source listing expiry: 20261231

Source-listed ingredients

URTICA DIOICA — 1 [hp_X]/77g
TOXICODENDRON PUBESCENS LEAF — 4 [hp_X]/77g
LEDUM PALUSTRE TWIG — 2 [hp_X]/77g

These values do not establish equivalence or a dose recommendation.

Packages

1 TUBE in 1 CARTON (68466-2001-8) / 77 g in 1 TUBE · 68466-2001-8

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.

Browse United States records →