United States · FDA National Drug Code directory

GUNA-ORAL

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
17089-452_7e8ff906-fbc2-e1bf-e053-2a91aa0a3326
Product NDC
17089-452
Form
SPRAY
Composition / generic term
ACHILLEA MILLEFOLIUM - ACONITUM NAPELLUS - ARNICA MONTANA - ATROPA BELLADONNA - CALCIUM SULFIDE - COMFREY ROOT - ECHINACEA ANGUSTIFOLIA - ECHINACEA PURPUREA - HYPERICUM PERFORATUM - SUS SCROFA TOOTH - WITCH HAZEL -
Labeler
Guna spa
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20100527
Source listing expiry
20261231

Source-listed ingredients

  • ACONITUM NAPELLUS — 3 [hp_X]/30mL
  • ARNICA MONTANA — 3 [hp_X]/30mL
  • ATROPA BELLADONNA — 4 [hp_X]/30mL
  • ECHINACEA ANGUSTIFOLIA — 2 [hp_X]/30mL
  • ECHINACEA PURPUREA — 2 [hp_X]/30mL
  • WITCH HAZEL — 2 [hp_X]/30mL
  • CALCIUM SULFIDE — 6 [hp_X]/30mL
  • HYPERICUM PERFORATUM — 3 [hp_X]/30mL
  • ACHILLEA MILLEFOLIUM — 3 [hp_X]/30mL
  • COMFREY ROOT — 6 [hp_X]/30mL
  • SUS SCROFA TOOTH — 12 [hp_X]/30mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, SPRAY in 1 BOX (17089-452-27) / 50 mL in 1 BOTTLE, SPRAY · 17089-452-27

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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