Label: CODEINUM- codeine pellet

  • Category: HUMAN PRESCRIPTION DRUG LABEL

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 7, 2023

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • SPL UNCLASSIFIED SECTION

    CII

  • WARNING

    "The FDA has not determined that the product is safe, effective and not misbranded for its intended use"

  • INDICATION:

    VERTIGO, DIARRHEA, PAIN OR OTHER INDICATIONS

  • WARNING:

    Use only if cap and seal are unbroken. Keep this and all medication out of reach of children. If symptoms persist for more than 3 days or worsen, discontinue (STOP) use and consult your physician. As with any drug. If you are pregnant or nursing (breast-feeding) a baby, seek the advise of a health professional before using this product. Store tightly closed in a cool area.

  • Directions (adult/children)

    Dissolve 3 or 4 pellets in mouth or under tongue 3 times a day or as directed by a physician. Children 2 years and older take 1/2 adult dose.

  • Inactive Ingredients

    Lactose and Sucrose. Free from yeast, wheat, corn and soy.

  • Other Information

    Contains approx. 170 - 172 pellets.

  • Questions or comments:

    (877) REM4YOU Fax (909) 594-4205 Pomona, Ca. 91768 USA www.remedymakers.com

  • WARNINGS AND PRECAUTIONS

    CAUTION: Federal law prohibits dispensing withhout prescription.

  • PRINCIPAL DISPLAY PANEL

    CODEINUM9X

  • INGREDIENTS AND APPEARANCE
    CODEINUM 
    codeine pellet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:10191-1035
    Route of AdministrationSUBLINGUALDEA ScheduleCII    
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CODEINE ANHYDROUS (UNII: UX6OWY2V7J) (CODEINE ANHYDROUS - UNII:UX6OWY2V7J) CODEINE ANHYDROUS9 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    LACTOSE (UNII: J2B2A4N98G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10191-1035-2170 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/14/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/14/2015
    Labeler - Remedy Makers (018543582)