United States · FDA National Drug Code directory

Dizziness HP

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 44911-0187_f02fda13-544f-409a-bb7b-038d49cf4932
Product NDC: 44911-0187
Form: LIQUID
Composition / generic term: Calcarea carbonica, Chenopodium anthelminticum, Cocculus indicus, Conium maculatum, Nux vomica, Phosphorus, Pulsatilla (pratensis), Silicea, Tabacum,
Labeler: Energique, Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start / end (source format): 20150708
Source listing expiry: 20261231

Source-listed ingredients

OYSTER SHELL CALCIUM CARBONATE, CRUDE — 30 [hp_X]/mL
DYSPHANIA AMBROSIOIDES — 30 [hp_X]/mL
ANAMIRTA COCCULUS SEED — 30 [hp_X]/mL
CONIUM MACULATUM FLOWERING TOP — 30 [hp_X]/mL
STRYCHNOS NUX-VOMICA SEED — 30 [hp_X]/mL
PHOSPHORUS — 30 [hp_X]/mL
PULSATILLA PRATENSIS WHOLE — 30 [hp_X]/mL
SILICON DIOXIDE — 30 [hp_X]/mL
TOBACCO LEAF — 30 [hp_X]/mL

These values do not establish equivalence or a dose recommendation.

Packages

30 mL in 1 BOTTLE, DROPPER (44911-0187-1) · 44911-0187-1

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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