Label: LYME DISEASE SUPPORT 1- alumen, calcarea carbonica, dna, ferrum phosphoricum, hepar sulphuris calcareum, kali carbonicum, kali muriaticum, kali sulphuricum, magnesia phosphorica, natrum muriaticum, natrum phosphoricum, rna, silicea. 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 December 29, 2021

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

View All Sections
  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS: Equal amounts of: Alumen 12X, Calcarea carbonica 6X, DNA 4C, Ferrum phosphoricum 6X, Hepar sulphuris calcareum 6X, Kali carbonicum 6X, Kali muriaticum 6X, Kali sulphuricum 6X, Magnesia phosphorica 6X, Natrum muriaticum 6X, Natrum phosphoricum 6X, RNA 4C, Silicea 12X.

  • INDICATIONS & USAGE

    USES: Supports the immune systems response to Lyme disease symptoms.*

    * ​Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

  • WARNINGS

    WARNINGS: iF PREGNANT OR BREAST-FEEDING, ask a health care professional before use. If symptoms worsen or persist for more than a week, discontinue use and contact a doctor.

    • ​KEEP OUT OF REACH OF CHILDREN.
  • DOSAGE & ADMINISTRATION

    DIRECTIONS: Shake bottle 10 times prior to each use. Adults & children above 12 years of age: Take 10 drops under the tongue 3 times per day or as directed by a health care practioner. Children under 12: Consult a health care provider.

  • OTHER SAFETY INFORMATION

    Do not use if cap seal is broken.

  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS: Ethanol Alcohol 15% (non-GMO, Kosher Certified, Cane, Gluten, Allergen Free), Vegetable Glycerin 15%, Purified Water.

  • QUESTIONS

    Mfg. By: OHM PHARMA, INC. Mineral Wells, TX 76067

    www.ohmpharma.com

  • PRINCIPAL DISPLAY PANEL

    HOMEOPATHIC MEDICINE

    NDC: 66096-722-05

    LYME DISEASE Support #1

    Natural - Safe - Effective

    No Side Effects

    2 fl oz (59mL) / 15% Alcohol

    PRODUCT OF USA

    2oz bottle label

    Supports the immune systems response to Lyme disease symptom

  • INGREDIENTS AND APPEARANCE
    LYME DISEASE SUPPORT 1 
    alumen, calcarea carbonica, dna, ferrum phosphoricum, hepar sulphuris calcareum, kali carbonicum, kali muriaticum, kali sulphuricum, magnesia phosphorica, natrum muriaticum, natrum phosphoricum, rna, silicea. liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66096-722
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM ALUM (UNII: 1L24V9R23S) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) POTASSIUM ALUM12 [hp_X]  in 59 mL
    OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (OYSTER SHELL CALCIUM CARBONATE, CRUDE - UNII:2E32821G6I) OYSTER SHELL CALCIUM CARBONATE, CRUDE6 [hp_X]  in 59 mL
    HERRING SPERM DNA (UNII: 51FI676N6F) (HERRING SPERM DNA - UNII:51FI676N6F) HERRING SPERM DNA4 [hp_C]  in 59 mL
    FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) FERROSOFERRIC PHOSPHATE6 [hp_X]  in 59 mL
    CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE6 [hp_X]  in 59 mL
    POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE6 [hp_X]  in 59 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CATION6 [hp_X]  in 59 mL
    POTASSIUM SULFATE (UNII: 1K573LC5TV) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM SULFATE6 [hp_X]  in 59 mL
    MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE6 [hp_X]  in 59 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE6 [hp_X]  in 59 mL
    SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B) (PHOSPHATE ION - UNII:NK08V8K8HR) SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE6 [hp_X]  in 59 mL
    SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX) (SACCHAROMYCES CEREVISIAE RNA - UNII:J17GBZ5VGX) SACCHAROMYCES CEREVISIAE RNA4 [hp_C]  in 59 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE12 [hp_X]  in 59 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66096-722-0559 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product11/20/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic11/20/2017
    Labeler - OHM PHARMA INC. (030572478)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!