DailyMed - 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

NDC Code(s): 44911-0725-1
Packager: Energique, Inc.

Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated December 20, 2024

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ACTIVE INGREDIENTS:
(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 ...

(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.
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PURPOSE:
May temporarily relieve symptoms associated with household chemicals sensitivities, such as dizziness and headache.** **Claims based on traditional homeopathic practice, not accepted medical ...

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.
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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 ...

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.
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KEEP OUT OF REACH OF CHILDREN:
In case of overdose, get medical help or contact a Poison Control Center right away.

In case of overdose, get medical help or contact a Poison Control Center right away.
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DIRECTIONS:
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 ...

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.
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INDICATIONS:
May temporarily relieve symptoms associated with household chemicals sensitivities, such as dizziness and headache.** **Claims based on traditional homeopathic practice, not accepted medical ...

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.
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INACTIVE INGREDIENTS:
Demineralized water, 20% Ethanol.

Demineralized water, 20% Ethanol.
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QUESTIONS:
Dist. by Energique, Inc. 201 Apple Blvd - Woodbine, IA 51579 - 800-869-8078

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579

800-869-8078
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PACKAGE LABEL DISPLAY:(What is this?)
ENERGIQUE - since 1987 - HOMEOPATHIC REMEDY - HOUSEHOLD ANTIGENS - 1 fl. oz (30 ml)

ENERGIQUE

since 1987

HOMEOPATHIC REMEDY

HOUSEHOLD ANTIGENS

1 fl. oz (30 ml)

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INGREDIENTS AND APPEARANCE

Product Information

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:44911-0725
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACETONE (UNII: 1364PS73AF) (ACETONE - UNII:1364PS73AF)	ACETONE	9 [hp_X] in 1 mL
SODIUM TRIPOLYPHOSPHATE, UNSPECIFIED FORM (UNII: 5HK03SA80J) (TRIPOLYPHOSPHATE ION - UNII:5798IYA5AY)	SODIUM TRIPOLYPHOSPHATE, UNSPECIFIED FORM	9 [hp_X] in 1 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	9 [hp_X] in 1 mL
BENZENE (UNII: J64922108F) (BENZENE - UNII:J64922108F)	BENZENE	9 [hp_X] in 1 mL
AMMONIUM CHLORIDE (UNII: 01Q9PC255D) (AMMONIUM CATION - UNII:54S68520I4)	AMMONIUM CATION	9 [hp_X] in 1 mL
SODIUM LAURYL SULFATE (UNII: 368GB5141J) (LAURYL SULFATE - UNII:DIQ16UC154)	SODIUM LAURYL SULFATE	9 [hp_X] in 1 mL
TURPENTINE OIL (UNII: C5H0QJ6V7F) (TURPENTINE OIL - UNII:C5H0QJ6V7F)	TURPENTINE OIL	9 [hp_X] in 1 mL
BUTYL ACETATE (UNII: 464P5N1905) (BUTYL ACETATE - UNII:464P5N1905)	BUTYL ACETATE	9 [hp_X] in 1 mL
ETHYL ACETATE (UNII: 76845O8NMZ) (ETHYL ACETATE - UNII:76845O8NMZ)	ETHYL ACETATE	9 [hp_X] in 1 mL
TOLUENE (UNII: 3FPU23BG52) (TOLUENE - UNII:3FPU23BG52)	TOLUENE	9 [hp_X] in 1 mL
XYLENE (MIXED ISOMERS) (UNII: D856J1047R) (XYLENE - UNII:D856J1047R)	XYLENE (MIXED ISOMERS)	9 [hp_X] in 1 mL
BISPHENOL A (UNII: MLT3645I99) (BISPHENOL A - UNII:MLT3645I99)	BISPHENOL A	9 [hp_X] in 1 mL
KEROSENE (UNII: 1C89KKC04E) (DEODORIZED KEROSENE - UNII:1C89KKC04E)	KEROSENE	9 [hp_X] in 1 mL
FORMALDEHYDE SOLUTION (UNII: T0H3L6C7I5) (FORMALDEHYDE SOLUTION - UNII:T0H3L6C7I5)	FORMALDEHYDE SOLUTION	9 [hp_X] in 1 mL
GLYPHOSATE (UNII: 4632WW1X5A) (GLYPHOSATE - UNII:4632WW1X5A)	GLYPHOSATE	9 [hp_X] in 1 mL
METHYLPARABEN (UNII: A2I8C7HI9T) (METHYLPARABEN - UNII:A2I8C7HI9T)	METHYLPARABEN	9 [hp_X] in 1 mL
NAPHTHALENE (UNII: 2166IN72UN) (NAPHTHALENE - UNII:2166IN72UN)	NAPHTHALENE	9 [hp_X] in 1 mL
PROPYLPARABEN (UNII: Z8IX2SC1OH) (PROPYLPARABEN - UNII:Z8IX2SC1OH)	PROPYLPARABEN	9 [hp_X] in 1 mL
SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU) (SEMECARPUS ANACARDIUM JUICE - UNII:Y0F0BU8RDU)	SEMECARPUS ANACARDIUM JUICE	12 [hp_X] in 1 mL
GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O)	GRAPHITE	12 [hp_X] in 1 mL
NITRIC ACID (UNII: 411VRN1TV4) (NITRIC ACID - UNII:411VRN1TV4)	NITRIC ACID	12 [hp_X] in 1 mL
PULSATILLA PRATENSIS WHOLE (UNII: 8E272251DI) (PULSATILLA PRATENSIS WHOLE - UNII:8E272251DI)	PULSATILLA PRATENSIS WHOLE	12 [hp_X] in 1 mL
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	12 [hp_X] in 1 mL
PARAFFIN (UNII: I9O0E3H2ZE) (PARAFFIN - UNII:I9O0E3H2ZE)	PARAFFIN	12 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:44911-0725-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	12/20/2024

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		12/20/2024

Labeler - Energique, Inc. (789886132)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(44911-0725) , api manufacture(44911-0725) , label(44911-0725) , pack(44911-0725)

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