Home DailyMed 7f79058a-c35a-429a-be3c-4cff1d657087 Household Detox Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer Deseret Biologicals, Inc. | Apotheca Company
Effective date 2024-12-13
Label type HUMAN OTC DRUG LABEL
Version 1
Source full-release
Hydrated at 2026-06-01 02:29:36 Label at a glance# Product Household Detox
Active ingredient GARLIC, ALUMINUM OXIDE, ANTIPYRINE, BENZENE, BISPHENOL A, PHENOL, CARBON DISULFIDE, DIETHYLSTILBESTROL, 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN, ESTRONE, FORMALDEHYDE SOLUTION, GLYPHOSATE, METHYLPARABEN, NAPHTHALENE, PARAFFIN, KEROSENE, PHENACETIN, PTELEA TRIFOLIATA BARK, CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED, POLYTETRAFLUOROETHYLENE
Label structure 9 sections
Indications and uses • For the temporary relief of symptoms including: • symptoms of toxicity • headache • fatigue • body aches • skin complaints These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Dosage and administration 1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43742-2222-1 Household Detox 30 mL in 1 BOTTLE, DROPPER LIQUID 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43742-2222 HOUSEHOLD DETOX (ALLIUM SATIVUM, ALUMINA, ANTIPYRINUM, BENZINUM, BISPHENOL A, CARBOLICUM ACIDUM, CARBONEUM SULPHURATUM, DIETHYLSTILBESTROL, DIOXIN, FOLLICULINUM, FORMALINUM, GLYPHOSATE, METHYLPARABEN, NAPHTHALINUM, PARAFFINUM, PETROLEUM, PHENACETINUM, PTELEA TRIFOLIATA, SODIUM CARBOXYMETHYL CELLULOSE, TEFLON) LIQUID [DESERET BIOLOGICALS, INC.] 1 Current NDC, 1 package rows 20241215_7f79058a-c35a-429a-be3c-4cff1d657087.zip
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 27 matching rows.
Household Detox Allium Sativum, Alumina, Antipyrinum, Benzinum, Bisphenol A, Carbolicum Acidum, Carboneum Sulphuratum, Diethylstilbestrol, Dioxin, Folliculinum, Formalinum, Glyphosate, Methylparaben, Naphthalinum, Paraffinum, Petroleum, Phenacetinum, Ptelea Trifoliata, Sodium Carboxymethyl Cellulose, Teflon GARLIC ALUMINUM OXIDE ALUMINA ANTIPYRINE BENZENE BISPHENOL A PHENOL CARBON DISULFIDE DIETHYLSTILBESTROL 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN ESTRONE FORMALDEHYDE SOLUTION GLYPHOSATE METHYLPARABEN NAPHTHALENE PARAFFIN KEROSENE DEODORIZED KEROSENE PHENACETIN PTELEA TRIFOLIATA BARK CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED CARBOXYMETHYLCELLULOSE POLYTETRAFLUOROETHYLENE WATER ALCOHOL Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 22 matching rows.
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.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Household Detox ALLIUM SATIVUM, ALUMINA, ANTIPYRINUM, BENZINUM, BISPHENOL A, CARBOLICUM ACIDUM, CARBONEUM SULPHURATUM, DIETHYLSTILBESTROL, DIOXIN, FOLLICULINUM, FORMALINUM, GLYPHOSATE, METHYLPARABEN, NAPHTHALINUM, PARAFFINUM, PETROLEUM, PHENACETINUM, PTELEA TRIFOLIATA, SODIUM CARBOXYMETHYL CELLULOSE, TEFLON Deseret Biologicals, Inc. 7f79058a-c35a-429a-be3c-4cff1d657087 2024-12-13 Warnings Exact identifier ndc (package): 43742-2222-1 ndc (product): 43742-2222 ndc11 (package): 43742222201 spl id: 498c0781-09c0-48e6-81d5-f27c998a310c spl set id: 7f79058a-c35a-429a-be3c-4cff1d657087
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.