Cold Armor

Manufacturer
Ratis, LLC
Effective date
2022-03-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:06:48

Label at a glance#

ProductCold Armor
Active ingredientONION, GOLDENSEAL, STRYCHNOS NUX-VOMICA SEED, ANEMONE PRATENSIS, FERROSOFERRIC PHOSPHATE, ATROPA BELLADONNA, GELSEMIUM SEMPERVIRENS ROOT, POTASSIUM DICHROMATE
Label structure9 sections

Dosage and administration

Adults and children 6 years of age and older: 2 sprays 3 times a day or as needed. Children 3-6: 1 spray as above. For Children under 3, consult a doctor.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Allium Cepa 6X, Hydrastis Canadensis 6X, Nux Vomica 6X, Pulsatilla (Pratensis) 6X, Ferrum Phosphoricum 8X, Belladonna 12X, Gelsemium Sempervirens 12X, Kali Bichromicum 12X.

PURPOSE:

OTC - PURPOSE SECTION

Temporarily relieves stuffy and runny nose, coughing, congestion, body aches, fever, weakness, and minor sore throats. **

** These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

For oral use only.

If pregnant or breast-feeding, or if symptoms persist or worsen, ask a health care professional.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control center right away. Do not use if tamper evident seal is broken or missing.

Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult physician promptly.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 6 years of age and older: 2 sprays 3 times a day or as needed. Children 3-6: 1 spray as above. For Children under 3, consult a doctor.

INDICATIONS:

INDICATIONS & USAGE SECTION

Temporarily relieves stuffy and runny nose, coughing, congestion, body aches, fever, weakness, and minor sore throats. **

** These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Citric Acid, Demineralized Water, Ethanol, Glycerin.

QUESTIONS:

OTC - QUESTIONS SECTION

Visit HomeopathyStore.com or call (888) 405-7551. Distributed by: Ratis, LLC, 211 E. Lombard St, STE 303, Baltimore, MD 21202

PACKAGE LABLE DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 71753-1056-1

Anna's 

REMEDIES

Cold Armor

COLD RELIEF**

HOMEOPATHIC ORAL SPRAY

1FL. OZ (30ML)

COLD ARMORCOLD ARMOR

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

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71753-105671753-1056-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
15c02a5f-7137-454f-9c00-316fd7921003a3a3db35-880e-4061-90c6-87e4082e49722022-03-08WarningsExact identifier
spl id: 15c02a5f-7137-454f-9c00-316fd7921003
spl set id: a3a3db35-880e-4061-90c6-87e4082e4972

Reported adverse events (FAERS/openFDA)#

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