United States · FDA National Drug Code directory

GUNA HAY FEVER RELIEF

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
17089-476_d3322d60-dd44-8e96-e053-2995a90a54b0
Product NDC
17089-476
Form
PELLET
Composition / generic term
strychnos nux vomica seed - histamine dihydrochloride - manganese - schoenocaulon officinale seed - apis mellifera - arsenic trioxide - silver nitrate - onion - euphrasia stricta - galphimia glauca flowering top - sulfur -
Labeler
Guna spa
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20210217
Source listing expiry
20261231

Source-listed ingredients

  • STRYCHNOS NUX-VOMICA SEED — 4 [hp_X]/4g
  • HISTAMINE DIHYDROCHLORIDE — 200 [hp_X]/4g
  • MANGANESE — 8 [hp_X]/4g
  • SCHOENOCAULON OFFICINALE SEED — 6 [hp_X]/4g
  • ONION — 30 [hp_X]/4g
  • APIS MELLIFERA — 200 [hp_X]/4g
  • SILVER NITRATE — 6 [hp_X]/4g
  • EUPHRASIA STRICTA — 5 [hp_X]/4g
  • GALPHIMIA GLAUCA FLOWERING TOP — 4 [hp_X]/4g
  • SULFUR — 30 [hp_X]/4g
  • ARSENIC TRIOXIDE — 30 [hp_X]/4g

These values do not establish equivalence or a dose recommendation.

Packages

  • 2 TUBE in 1 BOX (17089-476-20) / 4 g in 1 TUBE · 17089-476-20
  • 1 TUBE in 1 BOX (17089-476-21) / 4 g in 1 TUBE · 17089-476-21

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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