Dementia Drops

FDA Drug Profile — Dementia Drops 2117

Dementia Drops is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Dementia Drops 2117. Available dosage form: liquid.

Drug Details

Generic Name
Dementia Drops
Brand Names
Dementia Drops 2117
Application Number
Sponsor
Professional Complementary Health Formulas
NDC Codes
1
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
TURNERA DIFFUSA LEAF, CELERY SEED, ANHYDROUS DIBASIC CALCIUM PHOSPHATE, HYOSCYAMUS NIGER, BARIUM CARBONATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, PHOSPHORIC ACID, ZINC, GOLD MONOIODIDE, PICRIC ACID, PHOSPHORUS, LILIUM LANCIFOLIUM WHOLE FLOWERING, SULFUR

Indications and Usage

INDICATIONS For temporary relief of irritability, anxiousness, mood swings, forgetfulness, or confusion.*

Warnings

WARNINGS Consult a doctor if condition worsens or if symptoms persist. 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.