Home FDA labels 3cc00ed9-9470-439d-ba3c-7f367bda7bc6 Household Antigens openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name Household Antigens
Generic name 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
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID 87c92497-8a51-4977-87fe-e0b4c6bafb19
SPL ID 3cc00ed9-9470-439d-ba3c-7f367bda7bc6
Version 3
Effective date 2024-09-27
Source export date 2026-09-28
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:19:35 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 26 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Household Antigens openfda.brand_name generic name 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 openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0536-1 openfda.package_ndc ndc product 44911-0536 openfda.product_ndc ndc11 package 44911053601 derived:openfda.package_ndc spl id 3cc00ed9-9470-439d-ba3c-7f367bda7bc6 id spl set id 87c92497-8a51-4977-87fe-e0b4c6bafb19 set_id unii 01Q9PC255D openfda.unii unii 6DC9Q167V3 openfda.unii unii D856J1047R openfda.unii unii 4QQN74LH4O openfda.unii unii 411VRN1TV4 openfda.unii unii 464P5N1905 openfda.unii unii 5HK03SA80J openfda.unii unii J64922108F openfda.unii unii 1364PS73AF openfda.unii unii 76845O8NMZ openfda.unii unii MLT3645I99 openfda.unii unii 8E272251DI openfda.unii unii 70FD1KFU70 openfda.unii unii 368GB5141J openfda.unii unii Y0F0BU8RDU openfda.unii unii 3FPU23BG52 openfda.unii unii 1C89KKC04E openfda.unii unii C5H0QJ6V7F openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings 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.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.