NDC 44911-0187 – Dizziness HP
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… · Liquid · Oral
Product NDC44911-0187
Product details
- Brand name
- Dizziness HP
- Generic name
- Calcarea carbonica, Chenopodium anthelminticum, Cocculus indicus, Conium maculatum, Nux vomica, Phosphorus, Pulsatilla (pratensis), Silicea, Tabacum,
- Labeler
- Energique, Inc.
- Dosage form
- Liquid
- Route
- Oral
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketed since
- July 8, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Non-Standardized Plant Allergenic Extract; Non-Standardized Plant Allergenic Extract
Active 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
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 44911-0187-1 | 30 mL in 1 BOTTLE, DROPPER (44911-0187-1) | Jul 8, 2015 |