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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