United States · FDA National Drug Code directory
Cold Armor
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
- 71753-1156_fb97f830-fce0-4a6d-81cf-ae5d2abe5de7
- Product NDC
- 71753-1156
- Form
- SPRAY
- Composition / generic term
- Allium Cepa, Hydrastis Canadensis, Pulsatilla (Pratensis), Dulcamara, Nux Vomica, Ferrum Phosphoricum, Gelsemium Sempervirens, Kali Bichromicum
- Labeler
- Ratis, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20230526
- Source listing expiry
- 20261231
Source-listed ingredients
- ONION — 6 [hp_X]/mL
- GOLDENSEAL — 6 [hp_X]/mL
- PULSATILLA PRATENSIS WHOLE — 6 [hp_X]/mL
- SOLANUM DULCAMARA TOP — 8 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED — 8 [hp_X]/mL
- FERROSOFERRIC PHOSPHATE — 12 [hp_X]/mL
- GELSEMIUM SEMPERVIRENS ROOT — 12 [hp_X]/mL
- POTASSIUM DICHROMATE — 12 [hp_X]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 mL in 1 BOTTLE, SPRAY (71753-1156-1) · 71753-1156-1
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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