Home FDA labels cda1180e-7f69-69b2-e053-2995a90a5015 Dr. Talbots Pain Inflammation Relief 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 Dr. Talbots Pain Inflammation Relief
Generic name ARNICA, BELLIS PERENNIS, CALENDULA OFFICINALIS, CHAMOMILLA, COFFEA CRUDA, HYPERICUM, MILLEFOLIUM, FERRUM PHOSPHORICUM, KALI MURIATICUM, MAGNESIA PHOSPHORICA
Manufacturer Talbot's Pharmaceuticals Family Products, LLC.
Product type HUMAN OTC DRUG
SPL set ID 91d57aae-7c68-cc4a-e053-2995a90aad9d
SPL ID cda1180e-7f69-69b2-e053-2995a90a5015
Version 3
Effective date 2021-10-05
Source export date 2026-09-28
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:15:19 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 · 20 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Dr. Talbots Pain Inflammation Relief openfda.brand_name generic name ARNICA, BELLIS PERENNIS, CALENDULA OFFICINALIS, CHAMOMILLA, COFFEA CRUDA, HYPERICUM, MILLEFOLIUM, FERRUM PHOSPHORICUM, KALI MURIATICUM, MAGNESIA PHOSPHORICA openfda.generic_name manufacturer name Talbot's Pharmaceuticals Family Products, LLC. openfda.manufacturer_name ndc package 70797-316-01 openfda.package_ndc ndc package 70797-316-04 openfda.package_ndc ndc product 70797-316 openfda.product_ndc ndc11 package 70797031601 derived:openfda.package_ndc ndc11 package 70797031604 derived:openfda.package_ndc spl id cda1180e-7f69-69b2-e053-2995a90a5015 id spl set id 91d57aae-7c68-cc4a-e053-2995a90aad9d set_id unii 2FXJ6SW4PK openfda.unii unii XK4IUX8MNB openfda.unii unii 3SW678MX72 openfda.unii unii O80TY208ZW openfda.unii unii 18E7415PXQ openfda.unii unii 2HU33I03UY openfda.unii unii 91GQH8I5F7 openfda.unii unii 660YQ98I10 openfda.unii unii A1Y870209Z openfda.unii unii G0R4UBI2ZZ 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 Stop use and ask doctor if: fever develops, worsens, or lasts more than 3 days pain gets worse or lasts more than 7 days other symptoms persist for more than 7 days or worsen Ask a doctor before use if you are taking a prescription drug or have a serious medical condition. Please consult your physician immediately for a worsening condition. Warning
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.