LYME DISEASE SUPPORT 2- argentum nitricum, astragalus menziesii, calcarea sulphurica, cuprum arsenicosum, dna, ferrum phosphoricum, kali muriaticum, kali sulphuricum, ledum palustre, magnesia phosphorica, rna, silicea. liquid

Lyme Disease Support 2 by

Drug Labeling and Warnings

Lyme Disease Support 2 by is a Homeopathic medication manufactured, distributed, or labeled by OHM PHARMA INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENTS: Equal amounts of: Argentum nitricum 6X, Astragalus menziesii 3X, Calcarea sulphurica 6X, Cuprum arsenicosum 12X, DNA 4C, Ferrum phosphoricum 6X, Kali muriaticum 6X, Kali sulphuricum 6X, Ledum palustre 1M, Magnesia phosphorica 6X, RNA 4C, Silicea 6X.

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: 66096-723-05

LYME DISEASE Support #2

Natural - Safe - Effective

No Side Effects

2 fl oz (59mL) / 15% Alcohol

PRODUCT OF USA

Supports the immune systems response to Lyme disease symptoms.

INGREDIENTS AND APPEARANCE

LYME DISEASE SUPPORT 2 
argentum nitricum, astragalus menziesii, calcarea sulphurica, cuprum arsenicosum, dna, ferrum phosphoricum, kali muriaticum, kali sulphuricum, ledum palustre, magnesia phosphorica, rna, silicea. liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66096-723
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A)	SILVER NITRATE	6 [hp_X]  in 59 mL
ASTRAGALUS NUTTALLII LEAF (UNII: NC1P15G4KZ) (ASTRAGALUS NUTTALLII LEAF - UNII:NC1P15G4KZ)	ASTRAGALUS NUTTALLII LEAF	3 [hp_X]  in 59 mL
CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM SULFATE ANHYDROUS	6 [hp_X]  in 59 mL
CUPRIC ARSENITE (UNII: SK8L60BCSQ) (CUPRIC CATION - UNII:8CBV67279L)	CUPRIC ARSENITE	12 [hp_X]  in 59 mL
HERRING SPERM DNA (UNII: 51FI676N6F) (HERRING SPERM DNA - UNII:51FI676N6F)	HERRING SPERM DNA	4 [hp_C]  in 59 mL
FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7)	FERROSOFERRIC PHOSPHATE	6 [hp_X]  in 59 mL
POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM CATION	6 [hp_X]  in 59 mL
POTASSIUM SULFATE (UNII: 1K573LC5TV) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM SULFATE	6 [hp_X]  in 59 mL
RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P)	RHODODENDRON TOMENTOSUM LEAFY TWIG	1 [hp_M]  in 59 mL
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838)	MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE	6 [hp_X]  in 59 mL
SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX) (SACCHAROMYCES CEREVISIAE RNA - UNII:J17GBZ5VGX)	SACCHAROMYCES CEREVISIAE RNA	4 [hp_C]  in 59 mL
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	6 [hp_X]  in 59 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66096-723-05	59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	11/20/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		11/20/2017

Labeler - OHM PHARMA INC. (030572478)

Registrant - OHM PHARMA INC. (030572478)

Establishment
Name	Address	ID/FEI	Business Operations
OHM PHARMA INC.		030572478	manufacture(66096-723)