Lyme Disease Support 2
Lyme Disease Support 2 is an FDA drug label for the active ingredient ARGENTUM NITRICUM, ASTRAGALUS MENZIESII, CALCAREA SULPHURICA, CUPRUM ARSENICOSUM, DNA, FERRUM PHOSPHORICUM, KALI MURIATICUM, KALI SULPHURICUM, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RNA, SILICEA. manufactured by OHM PHARMA INC. administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20211229.
- Generic name
- ARGENTUM NITRICUM, ASTRAGALUS MENZIESII, CALCAREA SULPHURICA, CUPRUM ARSENICOSUM, DNA, FERRUM PHOSPHORICUM, KALI MURIATICUM, KALI SULPHURICUM, LEDUM PALUSTRE, MAGNESIA PHOSPHORICA, RNA, SILICEA.
- Manufacturer
- OHM PHARMA INC.
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 66096-723
- Application
- N/A
- Label effective
- 20211229
Active ingredients
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.
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.
Contraindications
Not available.
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.
Adverse Reactions
Not available.