Home FDA labels 99572f2b-6667-460a-828f-2074e823f91f Trauma plus Gel 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 Trauma plus Gel
Generic name CALENDULA OFFICINALIS, ARNICA MONTANA, HYPERICUM PERFORATUM, SYMPHYTUM OFFICINALE, BELLIS PERENNIS, LEDUM PALUSTRE, SULPHURICUM ACIDUM, CALCAREA FLUORICA, FERRUM PHOSPHORICUM, RHUS TOX, RUTA GRAVEOLENS, NATRUM SULPHURICUM
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID 53f4232b-23d4-48dc-aa76-175fdebfc74f
SPL ID 99572f2b-6667-460a-828f-2074e823f91f
Version 3
Effective date 2026-05-06
Source export date 2026-10-12
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:29:09 Harmonized routes table Harmonized routes TOPICAL
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 Trauma plus Gel openfda.brand_name generic name CALENDULA OFFICINALIS, ARNICA MONTANA, HYPERICUM PERFORATUM, SYMPHYTUM OFFICINALE, BELLIS PERENNIS, LEDUM PALUSTRE, SULPHURICUM ACIDUM, CALCAREA FLUORICA, FERRUM PHOSPHORICUM, RHUS TOX, RUTA GRAVEOLENS, NATRUM SULPHURICUM openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0466-1 openfda.package_ndc ndc product 44911-0466 openfda.product_ndc ndc11 package 44911046601 derived:openfda.package_ndc spl id 99572f2b-6667-460a-828f-2074e823f91f id spl set id 53f4232b-23d4-48dc-aa76-175fdebfc74f set_id unii 877L01IZ0P openfda.unii unii XK4IUX8MNB openfda.unii unii O3B55K4YKI openfda.unii unii O80TY208ZW openfda.unii unii 0YPR65R21J openfda.unii unii 18E7415PXQ openfda.unii unii 2HU33I03UY openfda.unii unii N94C2U587S openfda.unii unii M9VVZ08EKQ openfda.unii unii 91GQH8I5F7 openfda.unii unii 6IO182RP7A openfda.unii unii O40UQP6WCF 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: For external use only. If an adverse reaction occurs, discontinue use. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, 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. Do not expose product to extreme temperatures.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.