Home FDA labels b4dd6692-6cb8-a808-e053-2995a90ade14 Aches - Pains 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 Aches - Pains
Generic name ACONITUM NAP., ARG. NIT., ARNICA, BRYONIA, COLCHICUM, GUAIACUM, HYPERICUM, KALMIA, PHOSPHORUS, PHYTOLACCA, PULSATILLA, RHUS TOXICODENDRON, RUTA, SARCOLACTICUM AC., STICTA, STRAMONIUM, HAMAMELIS, TARAXACUM,
Manufacturer Newton Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 7923c9ad-6078-f496-e053-2991aa0a15c4
SPL ID b4dd6692-6cb8-a808-e053-2995a90ade14
Version 3
Effective date 2020-11-24
Source export date 2026-09-28
Source partition 14
Source file https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:40:16 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 · 30 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Aches - Pains openfda.brand_name generic name ACONITUM NAP., ARG. NIT., ARNICA, BRYONIA, COLCHICUM, GUAIACUM, HYPERICUM, KALMIA, PHOSPHORUS, PHYTOLACCA, PULSATILLA, RHUS TOXICODENDRON, RUTA, SARCOLACTICUM AC., STICTA, STRAMONIUM, HAMAMELIS, TARAXACUM, openfda.generic_name manufacturer name Newton Laboratories, Inc. openfda.manufacturer_name ndc package 55714-2382-1 openfda.package_ndc ndc package 55714-2382-2 openfda.package_ndc ndc package 55714-2382-0 openfda.package_ndc ndc product 55714-2382 openfda.product_ndc ndc11 package 55714238201 derived:openfda.package_ndc ndc11 package 55714238202 derived:openfda.package_ndc ndc11 package 55714238200 derived:openfda.package_ndc spl id b4dd6692-6cb8-a808-e053-2995a90ade14 id spl set id 7923c9ad-6078-f496-e053-2991aa0a15c4 set_id unii 27YLU75U4W openfda.unii unii 11E6VI8VEG openfda.unii unii XK4IUX8MNB openfda.unii unii 993QHL78E6 openfda.unii unii O80TY208ZW openfda.unii unii 79N6542N18 openfda.unii unii 03C8A0DFJ8 openfda.unii unii 39981FM375 openfda.unii unii N94C2U587S openfda.unii unii F9S9FFU82N openfda.unii unii 95IT3W8JZE openfda.unii unii 6IO182RP7A openfda.unii unii T7J046YI2B openfda.unii unii U0NQ8555JD openfda.unii unii G6W4F0V8Z3 openfda.unii unii I76KB35JEV openfda.unii unii T7S323PKJS openfda.unii unii D1YM0P5Z2T 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 SECTION Warnings: Keep our of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.