Cold HP
- Product NDC
- 44911-0089
- 11-digit product format
- 449110089
- Labeler code
- 44911
- Product ID
- 44911-0089_3df7f1a2-3c74-4d4d-ae78-ede87ce360c1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum Napellus, Allium Cepa, Eupatorium Perfoliatum, Ferrum Phosphoricum, Gelsemium Sempervirens, Kali Bichromicum, Mercurius Solubilis, Nux Vomica, Pulsatilla (Vulgaris)
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-08-21
- Substance
- ACONITUM NAPELLUS WHOLE; EUPATORIUM PERFOLIATUM FLOWERING TOP; FERRUM PHOSPHORICUM; GELSEMIUM SEMPERVIRENS ROOT; MERCURIUS SOLUBILIS; ONION; POTASSIUM DICHROMATE; PULSATILLA VULGARIS; STRYCHNOS NUX-VOMICA SEED
- 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], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Vegetable 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
- Cold HP
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ACONITUM NAPELLUS WHOLE | 30 [hp_X]/mL |
| EUPATORIUM PERFOLIATUM FLOWERING TOP | 30 [hp_X]/mL |
| FERRUM PHOSPHORICUM | 30 [hp_X]/mL |
| GELSEMIUM SEMPERVIRENS ROOT | 30 [hp_X]/mL |
| MERCURIUS SOLUBILIS | 30 [hp_X]/mL |
| ONION | 30 [hp_X]/mL |
| POTASSIUM DICHROMATE | 30 [hp_X]/mL |
| PULSATILLA VULGARIS | 30 [hp_X]/mL |
| STRYCHNOS NUX-VOMICA SEED | 30 [hp_X]/mL |
Harmonized Identifiers#
| Field | Values |
|---|---|
| Unii | U0NQ8555JD, 1W0775VX6E, 91GQH8I5F7, 639KR60Q1Q, 324Y4038G2, 492225Q21H, T4423S18FM, I76KB35JEV, 269XH13919 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 44911-0089-1 | 2024-10-24 | C162847 | 48780-1 | d6a99b39-5f33-a426-e053-dadaa90af4c2 | DRUG FACTS: |
| 44911-0089-1 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-5f33-a426-e053-dadaa90af4c2 | DRUG FACTS: |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 44911-0089-1 | Cold HP | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 44911-0089 | COLD HP (ACONITUM NAPELLUS, ALLIUM CEPA, EUPATORIUM PERFOLIATUM, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUM, MERCURIUS SOLUBILIS, NUX VOMICA, PULSATILLA (VULGARIS)) LIQUID [ENERGIQUE, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241027_d13b3de8-b1bc-41bd-a964-c3d8ba9f29fd.zip |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 44911-0089-1 | 44911008901 | 30 mL in 1 BOTTLE, DROPPER (44911-0089-1) | 30 ml | 2013-08-21 | 0000-00-00 | No | No | Current |