Household Antigens
- Manufacturer
- Energique, Inc. | Apotheca Company
- Effective date
- 2020-07-20
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:53:48
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
ACTIVE INGREDIENTS: Household Antigens 9X, 12X, 15X, 30X, Anacardium Orientale 12X, 15X, Grephites 12X, 15X, Nitriucm Acidum 12X, 15X, Pulsatilla 12X, 15X, Sulphur 15X.
OTC - PURPOSE SECTION
INDICATIONS: For temporary relief of allergies due to household chemicals.
WARNINGS SECTION
WARNINGS: 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.
DOSAGE & ADMINISTRATION SECTION
DIRECTIONS: Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care porfessional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.
INACTIVE INGREDIENT SECTION
INACTIVE INGREDIENTS: Demineralized water, 20% Ethanol.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.
INDICATIONS & USAGE SECTION
INDICATIONS: For temporary relief of allergies due to household chemicals.
OTC - QUESTIONS SECTION
Dist. by Energique, Inc.
201 Apple Blvd
Woodbine, IA 51579
800-869-8078
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
ENERGIQUE
since 1987
HOMEOPATHIC REMEDY
HOUSEHOLD ANTIGENS
1 fl. oz (30 ml)
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 44911-0017-1 | 2021-02-06 | C162847 | 48780-1 | 9d75b9d0-068b-f424-e053-dadaa90a57ce | Drug Facts: |
| 44911-0017-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-068b-f424-e053-dadaa90a57ce | Drug Facts: |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ACETONE | ACTIVE INGREDIENT | 1364PS73AF | 1 | |
| AMMONIUM CHLORIDE | ACTIVE INGREDIENT | 01Q9PC255D | 1 | |
| BUTYL ACETATE | ACTIVE INGREDIENT | 464P5N1905 | 1 | |
| DIBUTYL PHTHALATE | ACTIVE INGREDIENT | 2286E5R2KE | 1 | |
| ETHYL ACETATE | ACTIVE INGREDIENT | 76845O8NMZ | 1 | |
| GRAPHITE | ACTIVE INGREDIENT | 4QQN74LH4O | 1 | |
| KEROSENE | ACTIVE INGREDIENT | 1C89KKC04E | 1 | |
| NITRIC ACID | ACTIVE INGREDIENT | 411VRN1TV4 | 1 | |
| PROPYLENE GLYCOL | ACTIVE INGREDIENT | 6DC9Q167V3 | 1 | |
| PULSATILLA VULGARIS | ACTIVE INGREDIENT | I76KB35JEV | 1 | |
| SEMECARPUS ANACARDIUM JUICE | ACTIVE INGREDIENT | Y0F0BU8RDU | 1 | |
| SODIUM BENZENESULFONATE | ACTIVE INGREDIENT | K5RM14AZHX | 1 | |
| SODIUM LAURYL SULFATE | ACTIVE INGREDIENT | 368GB5141J | 1 | |
| SODIUM TRIPOLYPHOSPHATE | ACTIVE INGREDIENT | 5HK03SA80J | 1 | |
| SULFUR | ACTIVE INGREDIENT | 70FD1KFU70 | 1 | |
| TOLUENE | ACTIVE INGREDIENT | 3FPU23BG52 | 1 | |
| TURPENTINE OIL | ACTIVE INGREDIENT | C5H0QJ6V7F | 1 | |
| XYLENE | ACTIVE INGREDIENT | D856J1047R | 1 | |
| ACETONE | ACTIVE MOIETY | 1364PS73AF | 1 | |
| AMMONIUM CATION | ACTIVE MOIETY | 54S68520I4 | 1 | |
| BUTYL ACETATE | ACTIVE MOIETY | 464P5N1905 | 1 | |
| DIBUTYL PHTHALATE | ACTIVE MOIETY | 2286E5R2KE | 1 | |
| ETHYL ACETATE | ACTIVE MOIETY | 76845O8NMZ | 1 | |
| GRAPHITE | ACTIVE MOIETY | 4QQN74LH4O | 1 | |
| KEROSENE | ACTIVE MOIETY | 1C89KKC04E | 1 | |
| LAURYL SULFATE | ACTIVE MOIETY | DIQ16UC154 | 1 | |
| NITRIC ACID | ACTIVE MOIETY | 411VRN1TV4 | 1 | |
| PROPYLENE GLYCOL | ACTIVE MOIETY | 6DC9Q167V3 | 1 | |
| PULSATILLA VULGARIS | ACTIVE MOIETY | I76KB35JEV | 1 | |
| SEMECARPUS ANACARDIUM JUICE | ACTIVE MOIETY | Y0F0BU8RDU | 1 | |
| SODIUM BENZENESULFONATE | ACTIVE MOIETY | K5RM14AZHX | 1 | |
| SULFUR | ACTIVE MOIETY | 70FD1KFU70 | 1 | |
| TOLUENE | ACTIVE MOIETY | 3FPU23BG52 | 1 | |
| TRIPOLYPHOSPHATE ION | ACTIVE MOIETY | 5798IYA5AY | 1 | |
| TURPENTINE OIL | ACTIVE MOIETY | C5H0QJ6V7F | 1 | |
| XYLENE | ACTIVE MOIETY | D856J1047R | 1 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 1 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- Household Antigens
- Acetone, Sodium tripolyphosphate, Propylene glycol, Sodium benzene sulfonate, Sodium lauryl sulfate, Terebinthina,
- ACETONE
- SODIUM TRIPOLYPHOSPHATE
- TRIPOLYPHOSPHATE ION
- PROPYLENE GLYCOL
- SODIUM BENZENESULFONATE
- BENZENESULFONIC ACID -
- AMMONIUM CHLORIDE
- AMMONIUM CATION
- SODIUM LAURYL SULFATE
- LAURYL SULFATE
- TURPENTINE OIL
- BUTYL ACETATE
- TOLUENE
- XYLENE (MIXED ISOMERS)
- XYLENE
- DIBUTYL PHTHALATE
- KEROSENE
- SEMECARPUS ANACARDIUM JUICE
- GRAPHITE
- NITRIC ACID
- PULSATILLA VULGARIS WHOLE
- ANEMONE PULSATILLA
- SULFUR
- ETHYL ACETATE
- Water
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 44911-0017 | 44911-0017-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACETONE | 1364PS73AF | ACTIB |
| SODIUM TRIPOLYPHOSPHATE | 5HK03SA80J | ACTIB |
| PROPYLENE GLYCOL | 6DC9Q167V3 | ACTIB |
| SODIUM BENZENESULFONATE | K5RM14AZHX | ACTIB |
| AMMONIUM CHLORIDE | 01Q9PC255D | ACTIM |
| SODIUM LAURYL SULFATE | 368GB5141J | ACTIB |
| TURPENTINE OIL | C5H0QJ6V7F | ACTIB |
| BUTYL ACETATE | 464P5N1905 | ACTIB |
| TOLUENE | 3FPU23BG52 | ACTIB |
| XYLENE (MIXED ISOMERS) | D856J1047R | ACTIB |
| DIBUTYL PHTHALATE | 2286E5R2KE | ACTIB |
| KEROSENE | 1C89KKC04E | ACTIB |
| SEMECARPUS ANACARDIUM JUICE | Y0F0BU8RDU | ACTIB |
| GRAPHITE | 4QQN74LH4O | ACTIB |
| NITRIC ACID | 411VRN1TV4 | ACTIB |
| PULSATILLA VULGARIS WHOLE | I76KB35JEV | ACTIB |
| SULFUR | 70FD1KFU70 | ACTIB |
| ETHYL ACETATE | 76845O8NMZ | ACTIB |
| Water | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
Source Document#
Inactive ingredient matches#
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 | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg |
openFDA label cross-check#
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 |
|---|---|---|---|---|---|---|
| bc799447-8a97-4831-ba60-2131a1c616c8 | 137b3c35-1213-4dd7-9da9-ca5aa8329bb5 | 2020-07-20 | Warnings | bc799447-8a97-4831-ba60-2131a1c616c8 137b3c35-1213-4dd7-9da9-ca5aa8329bb5 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
