Dizziness
- Product NDC
- 44911-0187
- 11-digit product format
- 449110187
- Labeler code
- 44911
- Product ID
- 44911-0187_f02fda13-544f-409a-bb7b-038d49cf4932
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calcarea carbonica, Chenopodium anthelminticum, Cocculus indicus, Conium maculatum, Nux vomica, Phosphorus, Pulsatilla (pratensis), Silicea, Tabacum,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-07-08
- Substance
- ANAMIRTA COCCULUS SEED; CONIUM MACULATUM FLOWERING TOP; DYSPHANIA AMBROSIOIDES; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; PULSATILLA PRATENSIS WHOLE; SILICON DIOXIDE; STRYCHNOS NUX-VOMICA SEED; TOBACCO LEAF
- Active strength
- 30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dizziness
- Brand name suffix
- HP
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ANAMIRTA COCCULUS SEED | 30 [hp_X]/mL |
| CONIUM MACULATUM FLOWERING TOP | 30 [hp_X]/mL |
| DYSPHANIA AMBROSIOIDES | 30 [hp_X]/mL |
| OYSTER SHELL CALCIUM CARBONATE, CRUDE | 30 [hp_X]/mL |
| PHOSPHORUS | 30 [hp_X]/mL |
| PULSATILLA PRATENSIS WHOLE | 30 [hp_X]/mL |
| SILICON DIOXIDE | 30 [hp_X]/mL |
| STRYCHNOS NUX-VOMICA SEED | 30 [hp_X]/mL |
| TOBACCO LEAF | 30 [hp_X]/mL |
Harmonized Identifiers#
| Field | Values |
|---|---|
| Unii | 810258W28U, Q28R5GF371, 4H5RSU087I, 2E32821G6I, 27YLU75U4W, 8E272251DI, ETJ7Z6XBU4, 269XH13919, 6YR2608RSU |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 7792dadb-52b6-46b6-8fdf-80b1171065b5 | Product name | 1 | 20180810 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 44911-0187-1 | 2025-11-19 | C162847 | 48780-1 | 1030e365-1511-111a-e063-dadaa90a10e2 | DRUG FACTS: |
| 44911-0187-1 | 2024-01-30 | C162847 | 48780-1 | 1030e365-1511-111a-e063-dadaa90a10e2 | DRUG FACTS: |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 44911-0187-1 | DizzinessHP | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 44911-0187 | DIZZINESS HP (CALCAREA CARBONICA, CHENOPODIUM ANTHELMINTICUM, COCCULUS INDICUS, CONIUM MACULATUM, NUX VOMICA, PHOSPHORUS, PULSATILLA (PRATENSIS), SILICEA, TABACUM,) LIQUID [ENERGIQUE, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20220304_0bf53ecc-c2ad-40b5-b921-7c10a1b00626.zip |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 44911-0187-1 | 44911018701 | 30 mL in 1 BOTTLE, DROPPER (44911-0187-1) | 30 ml | 2015-07-08 | 0000-00-00 | No | No | Current |