Lyme Nosode Drops

FDA Drug Profile — Lyme Nosode Drops 2128

Lyme Nosode Drops is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Lyme Nosode Drops 2128. Available dosage form: liquid.

Drug Details

Generic Name
Lyme Nosode Drops
Brand Names
Lyme Nosode Drops 2128
Application Number
Sponsor
Professional Complementary Health Formulas
NDC Codes
1
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
ANGELICA ARCHANGELICA ROOT, ANGELICA PUBESCENS ROOT, GAMBIR, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, POTASSIUM CHLORIDE, MANGANESE, YUCCA FILAMENTOSA WHOLE, BOVINE TYPE II COLLAGEN (TRACHEAL CARTILAGE), PHYTOLACCA AMERICANA ROOT, GOLDENSEAL, TOXICODENDRON PUBESCENS LEAF, CAUSTICUM, LATIGLUTENASE, OXALIC ACID, ARNICA MONTANA WHOLE, LATRODECTUS MACTANS, BORRELIA BURGDORFERI, TREPONEMIC SKIN CANKER HUMAN, RICKETTSIA AKARI, BABESIA MICROTI, EHRLICHIA CHAFFEENSIS

Indications and Usage

INDICATIONS For the temporary relief of minor aches in the muscles or joints, chills, sweats, fatigue, or nausea.*

Warnings

WARNINGS Persistent symptoms may be a sign of a serious condition. If symptoms persist or are accompanied by a fever, rash, or persistent headache, consult a doctor. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.