United States · FDA National Drug Code directory

GUNA-REFLUX

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
17089-406_7e8f7213-7f81-14ab-e053-2991aa0a4669
Product NDC
17089-406
Form
SOLUTION/ DROPS
Composition / generic term
ACTIVATED CHARCOAL - AETHUSA CYNAPIUM - APOMORPHINE HYDROCHLORIDE - BRYONIA ALBA ROOT - COLCHICUM AUTUMNALE BULB - IPECAC - LYCOPODIUM CLAVATUM SPORE - STRYCHNOS IGNATII SEED - STRYCHNOS NUX-VOMICA SEED - WATERMELON - SUS SCROFA STOMACH -
Labeler
Guna spa
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20100512
Source listing expiry
20261231

Source-listed ingredients

  • AETHUSA CYNAPIUM — 4 [hp_X]/30mL
  • APOMORPHINE HYDROCHLORIDE — 6 [hp_X]/30mL
  • BRYONIA ALBA ROOT — 30 [hp_X]/30mL
  • ACTIVATED CHARCOAL — 12 [hp_X]/30mL
  • SUS SCROFA STOMACH — 10 [hp_X]/30mL
  • COLCHICUM AUTUMNALE BULB — 6 [hp_X]/30mL
  • WATERMELON — 30 [hp_X]/30mL
  • SUS SCROFA ESOPHAGUS — 10 [hp_X]/30mL
  • STRYCHNOS IGNATII SEED — 6 [hp_X]/30mL
  • IPECAC — 4 [hp_X]/30mL
  • LYCOPODIUM CLAVATUM SPORE — 5 [hp_X]/30mL
  • STRYCHNOS NUX-VOMICA SEED — 4 [hp_X]/30mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, DROPPER in 1 BOX (17089-406-18) / 30 mL in 1 BOTTLE, DROPPER · 17089-406-18

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 →