Belladonna

FDA Drug Profile — Belladonna, BM Belladonna, Bestmade Natural Products Belladonna, Belladonna 7106, Belladonna 30X

Belladonna is listed in the FDA National Drug Code directory with 14 NDC codes, marketed under brand names including Belladonna, BM Belladonna, Bestmade Natural Products Belladonna. Available dosage forms: liquid, pellet, globule, tablet, soluble.

Drug Details

Generic Name
Belladonna
Brand Names
Belladonna, BM Belladonna, Bestmade Natural Products Belladonna, Belladonna 7106, Belladonna 30X
Application Number
Sponsor
Energique, Inc.
NDC Codes
14
Dosage Forms
LIQUID, PELLET, GLOBULE, TABLET, SOLUBLE
Routes
ORAL, SUBLINGUAL
Active Ingredients
ATROPA BELLADONNA, AMARYLLIS BELLADONNA WHOLE

Indications and Usage

INDICATIONS: May temporarily relieve fever, irritated throat, and acute irritation of the bladder.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings

WARNINGS: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place. Warning: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult physician promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by a physician.