Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care porfessional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.
(in each drop): 9.09% of Anacardium Orientale 12X, 15X, Graphites 12X, 15X, Nitricum Acidum 12X, 15X, Pulsatilla (Pratensis) 12X, 15X, Sulphur 12X, 15X; 2.27% of Acetone 9X, 12X, 15X, 30X, Sodium Tripolyphosphate 9X, 12X, 15X, 30X, Propylene Glycol 9X, 12X, 15X, 30X, Benzinum 9X, 12X, 15X, 30X, Ammonium Muriaticum 9X, 12X, 15X, 30X, Sodium Lauryl Sulfate 9X, 12X, 15X, 30X, Terebinthina 9X, 12X, 15X, 30X, Butyl Acetate 9X, 12X, 15X, 30X, Ethyl Acetate 9X, 12X, 15X, 30X, Toluene 9X, 12X, 15X, 30X, Xylene 9X, 12X, 15X, 30X, Bisphenol A 9X, 12X, 15X, 30X, Petroleum 9X, 12X, 15X, 30X.
May temporariy relieve symptoms associated with household chemicals sensitivities, such as dizziness and headache.**
**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.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care porfessional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.
May temporariy relieve symptoms associated with household chemicals sensitivities, such as dizziness and headache.**
**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Demineralized water, 20% Ethanol.
Dist. by Energique, Inc.
201 Apple Blvd
Woodbine, IA 51579
800-869-8078
ENERGIQUE
since 1987
HOMEOPATHIC REMEDY
HOUSEHOLD ANTIGENS
1 fl. oz (30 ml)
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 44911-0536-1 | 2024-09-27 | C162847 | 48780-1 | f386c64a-0001-0266-e053-dadaa90a7c1a | Drugs: |
| 44911-0536-1 | 2023-01-30 | C162847 | 48780-1 | f386c64a-0001-0266-e053-dadaa90a7c1a | Drugs: |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 44911-0536-1 | Household Antigens | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 3 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 44911-0536 | HOUSEHOLD ANTIGENS (ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, BUTYL ACETATE, ETHYL ACETATE, TOLUENE, XYLENE, BISPHENOL A, PETROLEUM, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHUR) LIQUID [ENERGIQUE, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20240929_87c92497-8a51-4977-87fe-e0b4c6bafb19.zip |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 44911-0536 | 44911-0536-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACETONE | 1364PS73AF | ACTIB |
| SODIUM TRIPOLYPHOSPHATE | 5HK03SA80J | ACTIB |
| PROPYLENE GLYCOL | 6DC9Q167V3 | ACTIB |
| BENZENE | J64922108F | ACTIB |
| AMMONIUM CHLORIDE | 01Q9PC255D | ACTIM |
| SODIUM LAURYL SULFATE | 368GB5141J | ACTIB |
| TURPENTINE OIL | C5H0QJ6V7F | ACTIB |
| BUTYL ACETATE | 464P5N1905 | ACTIB |
| ETHYL ACETATE | 76845O8NMZ | ACTIB |
| TOLUENE | 3FPU23BG52 | ACTIB |
| XYLENE (MIXED ISOMERS) | D856J1047R | ACTIB |
| BISPHENOL A | MLT3645I99 | ACTIB |
| KEROSENE | 1C89KKC04E | ACTIB |
| SEMECARPUS ANACARDIUM JUICE | Y0F0BU8RDU | ACTIB |
| GRAPHITE | 4QQN74LH4O | ACTIB |
| NITRIC ACID | 411VRN1TV4 | ACTIB |
| ANEMONE PRATENSIS | 8E272251DI | ACTIB |
| SULFUR | 70FD1KFU70 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
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 |
|---|---|---|---|---|---|---|
| Household Antigens | ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, BUTYL ACETATE, ETHYL ACETATE, TOLUENE, XYLENE, BISPHENOL A, PETROLEUM, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHUR | Energique, Inc. | 87c92497-8a51-4977-87fe-e0b4c6bafb19 | 2024-09-27 | Warnings | 44911-0536-1 44911-0536 44911053601 3cc00ed9-9470-439d-ba3c-7f367bda7bc6 87c92497-8a51-4977-87fe-e0b4c6bafb19 |
Adverse event summaries are temporarily unavailable. Other product information remains available.