United States · FDA National Drug Code directory
Cold Crush Adult
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
- 69676-0006_59a83a25-acaf-7b07-e063-6294a90a56d0
- Product NDC
- 69676-0006
- Form
- TABLET, CHEWABLE
- Composition / generic term
- Aconitum napellus, Allium cepa, Bryonia alba, Euphrasia officinalis, Gelsemium sempervirens, Nux vomica, Pulsatilla, Rhus toxicodendron, Sabadilla
- Labeler
- Genexa Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20180711
- Source listing expiry
- 20271231
Source-listed ingredients
- PULSATILLA PRATENSIS — 6 [hp_X]/1
- GELSEMIUM SEMPERVIRENS ROOT — 12 [hp_X]/1
- ONION — 6 [hp_X]/1
- ACONITUM NAPELLUS — 6 [hp_X]/1
- BRYONIA ALBA ROOT — 12 [hp_X]/1
- EUPHRASIA STRICTA — 6 [hp_X]/1
- TOXICODENDRON PUBESCENS SHOOT — 12 [hp_X]/1
- STRYCHNOS NUX-VOMICA SEED — 12 [hp_X]/1
- SCHOENOCAULON OFFICINALE SEED — 12 [hp_X]/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (69676-0006-1) / 60 TABLET, CHEWABLE in 1 BOTTLE · 69676-0006-1
- 2 TABLET, CHEWABLE in 1 POUCH (69676-0006-3) · 69676-0006-3
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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