Adults and children 5 to 10 drops orally, every 2 to 4 hours as needed for relief of symptoms or as otherwise directed by a health care professional. If symptoms persist for more than 2 days, consult your health care professional. Consult a physician for use in children under 12 years of age.
(in each drop): 11.11% of Aconitum Napellus 30X, Allium Cepa 30X, Eupatorium Perfoliatum 30X, Ferrum Phosphoricum 30X, Gelsemium Sempervirens 30X, Kali Bichromicum 30X, Mercurius Solubilis 30X, Nux Vomica 30X, Pulsatilla 30X.
May temporarily relieve symptoms of nasal congestion, runny nose, sneezing, irritated throat, fever/chills, and/or discharges.**
**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Do not use if tamper evident seal is broken or missing.
Store in a cool, dry place.
Severe or persistent sore throat or sore throat accompanied by fever, headache, nausea, and vomiting may be serious. Consult a physician promptly. Do not use more than two days or administer to children under 3 years of age unless directed by a physician.
Adults and children 5 to 10 drops orally, every 2 to 4 hours as needed for relief of symptoms or as otherwise directed by a health care professional. If symptoms persist for more than 2 days, consult your health care professional. Consult a physician for use in children under 12 years of age.
Demineralized water, 20% Ethanol.
In case of overdose, get medical help or contact a Poison Control Center right away.
May temporarily relieve symptoms of nasal congestion, runny nose, sneezing, irritated throat, fever/chills, and/or discharges.**
**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Dist. By Energique, Inc.
201 Apple Blvd.
Woodbine, IA 51579
800.869.8078
ENERGIQUE
SINCE 1987
HOMEOPATHIC REMEDY
COLD HP
1 fl. oz. (30 ml)
| 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: |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 44911-0089-1 | Cold HP | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 4 |
| 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 |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ACONITUM NAPELLUS | ACTIVE INGREDIENT | U0NQ8555JD | 1 | |
| EUPATORIUM PERFOLIATUM FLOWERING TOP | ACTIVE INGREDIENT | 1W0775VX6E | 1 | |
| FERRUM PHOSPHORICUM | ACTIVE INGREDIENT | 91GQH8I5F7 | 1 | |
| GELSEMIUM SEMPERVIRENS ROOT | ACTIVE INGREDIENT | 639KR60Q1Q | 1 | |
| MERCURIUS SOLUBILIS | ACTIVE INGREDIENT | 324Y4038G2 | 1 | |
| ONION | ACTIVE INGREDIENT | 492225Q21H | 1 | |
| POTASSIUM DICHROMATE | ACTIVE INGREDIENT | T4423S18FM | 1 | |
| PULSATILLA VULGARIS | ACTIVE INGREDIENT | I76KB35JEV | 1 | |
| STRYCHNOS NUX-VOMICA SEED | ACTIVE INGREDIENT | 269XH13919 | 1 | |
| ACONITUM NAPELLUS | ACTIVE MOIETY | U0NQ8555JD | 1 | |
| DICHROMATE ION | ACTIVE MOIETY | 9LKY4BFN2V | 1 | |
| EUPATORIUM PERFOLIATUM FLOWERING TOP | ACTIVE MOIETY | 1W0775VX6E | 1 | |
| FERROSOFERRIC PHOSPHATE | ACTIVE MOIETY | 91GQH8I5F7 | 1 | |
| GELSEMIUM SEMPERVIRENS ROOT | ACTIVE MOIETY | 639KR60Q1Q | 1 | |
| MERCURIUS SOLUBILIS | ACTIVE MOIETY | 324Y4038G2 | 1 | |
| ONION | ACTIVE MOIETY | 492225Q21H | 1 | |
| PULSATILLA VULGARIS | ACTIVE MOIETY | I76KB35JEV | 1 | |
| STRYCHNOS NUX-VOMICA SEED | ACTIVE MOIETY | 269XH13919 | 1 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 44911-0089 | 44911-0089-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACONITUM NAPELLUS WHOLE | U0NQ8555JD | ACTIB |
| ONION | 492225Q21H | ACTIB |
| EUPATORIUM PERFOLIATUM FLOWERING TOP | 1W0775VX6E | ACTIB |
| FERRUM PHOSPHORICUM | 91GQH8I5F7 | ACTIB |
| GELSEMIUM SEMPERVIRENS ROOT | 639KR60Q1Q | ACTIB |
| POTASSIUM DICHROMATE | T4423S18FM | ACTIB |
| MERCURIUS SOLUBILIS | 324Y4038G2 | ACTIB |
| STRYCHNOS NUX-VOMICA SEED | 269XH13919 | ACTIB |
| PULSATILLA VULGARIS | I76KB35JEV | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Cold HP | ACONITUM NAPELLUS, ALLIUM CEPA, EUPATORIUM PERFOLIATUM, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUM, MERCURIUS SOLUBILIS, NUX VOMICA, PULSATILLA (VULGARIS) | Energique, Inc. | d13b3de8-b1bc-41bd-a964-c3d8ba9f29fd | 2024-10-24 | Warnings | 44911-0089-1 44911-0089 44911008901 3df7f1a2-3c74-4d4d-ae78-ede87ce360c1 d13b3de8-b1bc-41bd-a964-c3d8ba9f29fd |
Adverse event summaries are temporarily unavailable. Other product information remains available.