Label: COLD ARMOR (allium cepa, hydrastis canadensis, nux vomica, pulsatilla- pratensis, ferrum phosphoricum, belladonna, gelsemium sempervirens, kali bichromicum liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated March 8, 2022

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENTS:

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

  • PURPOSE:

    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:

    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:

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

  • DIRECTIONS:

    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:

    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:

    Citric Acid, Demineralized Water, Ethanol, Glycerin.

  • QUESTIONS:

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

  • PACKAGE LABLE DISPLAY:

    NDC 71753-1056-1

    Anna's 

    REMEDIES

    Cold Armor

    COLD RELIEF**

    HOMEOPATHIC ORAL SPRAY

    1FL. OZ (30ML)

    COLD ARMOR

  • INGREDIENTS AND APPEARANCE
    COLD ARMOR 
    allium cepa, hydrastis canadensis, nux vomica, pulsatilla (pratensis), ferrum phosphoricum, belladonna, gelsemium sempervirens, kali bichromicum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71753-1056
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION6 [hp_X]  in 1 mL
    GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL6 [hp_X]  in 1 mL
    STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED6 [hp_X]  in 1 mL
    ANEMONE PRATENSIS (UNII: 8E272251DI) (ANEMONE PRATENSIS - UNII:8E272251DI) ANEMONE PRATENSIS6 [hp_X]  in 1 mL
    FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) FERROSOFERRIC PHOSPHATE8 [hp_X]  in 1 mL
    ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA12 [hp_X]  in 1 mL
    GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q) GELSEMIUM SEMPERVIRENS ROOT12 [hp_X]  in 1 mL
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE12 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71753-1056-130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/23/201909/15/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/23/201909/15/2025
    Labeler - Ratis, LLC (964594324)