Cold Armor

Product NDC
71753-1056
11-digit product format
717531056
Labeler code
71753
Product ID
71753-1056_15c02a5f-7137-454f-9c00-316fd7921003
Type
HUMAN OTC DRUG
Nonproprietary name
Allium Cepa, Hydrastis Canadensis, Nux Vomica, Pulsatilla (Pratensis), Ferrum Phosphoricum, Belladonna, Gelsemium Sempervirens, Kali Bichromicum
Dosage form
LIQUID
Route
ORAL
Labeler
Ratis, LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-09-23
Marketing end
2025-09-15
Substance
ANEMONE PRATENSIS; ATROPA BELLADONNA; FERROSOFERRIC PHOSPHATE; GELSEMIUM SEMPERVIRENS ROOT; GOLDENSEAL; ONION; POTASSIUM DICHROMATE; STRYCHNOS NUX-VOMICA SEED
Active strength
6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Vegetable Proteins [CS]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct71753-1056DDiscontinued by firm2026-10-05
excluded packagepackage71753-105671753-1056-1DDiscontinued by firm2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproduct71753-1056DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage71753-105671753-1056-1DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71753-1056COLD ARMOR (ALLIUM CEPA, HYDRASTIS CANADENSIS, NUX VOMICA, PULSATILLA (PRATENSIS), FERRUM PHOSPHORICUM, BELLADONNA, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUM) LIQUID [RATIS, LLC]3Legacy NDC20220309_a3a3db35-880e-4061-90c6-87e4082e4972.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71753-1056-17175310560130 mL in 1 BOTTLE, SPRAY (71753-1056-1) 30 ml2019-09-232025-09-15NoNoCurrent