Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. 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): 6.66% of Anacardium Orientale, Graphites, Nitricum Acidum, Pulsatilla, Sulphur 12X, 15X; Paraffinum 12X, 15X, 30X. 1.67% of Household Allersodes (Acetone, Ammonium Muriaticum, Benzinum, Bisphenol A, Butyl Acetate, Ethyl Acetate, Petroleum, Propylene Glycol, Sodium Lauryl Sulfate, Sodium Tripolyphosphate, Terebinthina, Toluene, Xylene), Household Allersodes II (Formalinum, Glyphosate, Methylparaben, Naphthalinum, Propylparaben), 9X, 12X, 15X, 30X.
May temporarily 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.
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 professional. 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 temporarily 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)
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 44911-0725-1 | Household Antigens | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 1 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 44911-0725 | HOUSEHOLD ANTIGENS (ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, BUTYL ACETATE, ETHYL ACETATE, TOLUENE, XYLENE, BISPHENOL A, PETROLEUM, FORMALINUM, GLYPHOSATE, METHYLPARABEN, NAPHTHALINUM, PROPYLPARABEN, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHUR, PARAFFINUM) LIQUID [ENERGIQUE, INC.] | 1 | Current NDC, 1 package rows | 20241228_f3db63df-62a4-48d6-92e7-94e4a5701552.zip |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 44911-0725 | 44911-0725-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACETONE | 1364PS73AF | ACTIB |
| SODIUM TRIPOLYPHOSPHATE, UNSPECIFIED FORM | 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 |
| FORMALDEHYDE SOLUTION | T0H3L6C7I5 | ACTIB |
| GLYPHOSATE | 4632WW1X5A | ACTIB |
| METHYLPARABEN | A2I8C7HI9T | ACTIB |
| NAPHTHALENE | 2166IN72UN | ACTIB |
| PROPYLPARABEN | Z8IX2SC1OH | ACTIB |
| SEMECARPUS ANACARDIUM JUICE | Y0F0BU8RDU | ACTIB |
| GRAPHITE | 4QQN74LH4O | ACTIB |
| NITRIC ACID | 411VRN1TV4 | ACTIB |
| PULSATILLA PRATENSIS WHOLE | 8E272251DI | ACTIB |
| SULFUR | 70FD1KFU70 | ACTIB |
| PARAFFIN | I9O0E3H2ZE | 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, FORMALINUM, GLYPHOSATE, METHYLPARABEN, NAPHTHALINUM, PROPYLPARABEN, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHUR, PARAFFINUM | Energique, Inc. | f3db63df-62a4-48d6-92e7-94e4a5701552 | 2024-12-20 | Warnings | 44911-0725-1 44911-0725 44911072501 037a3c93-3157-4424-a28d-b8445eb46d6e f3db63df-62a4-48d6-92e7-94e4a5701552 |
Adverse event summaries are temporarily unavailable. Other product information remains available.