Muscle-Tendon

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: Muscle-Tendon
Generic name: ACONITUM NAP., ANTIMON. TART.,ARG. NIT., ARNICA, BRYONIA, CHAMOMILLA,CHELIDONIUM MAJUS, CIMICIFUGA, EUPATORIUM PERF.,HYPERICUM, NUX VOM., RHUS TOXICODENDRON, RUTA,SARCOLACTICUM AC., STRAMONIUM, STRYCHNINUM,CHAMOMILLA, PHYTOLACCA, RUTA, SYMPHYTUM.
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 9960c87f-f299-5d92-e053-2a95a90a7012
SPL ID: b5ab99d9-2e9f-5578-e053-2995a90a81b3
Version: 2
Effective date: 2020-12-04
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:18:04

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		Muscle-Tendon	openfda.brand_name
generic name		ACONITUM NAP., ANTIMON. TART.,ARG. NIT., ARNICA, BRYONIA, CHAMOMILLA,CHELIDONIUM MAJUS, CIMICIFUGA, EUPATORIUM PERF.,HYPERICUM, NUX VOM., RHUS TOXICODENDRON, RUTA,SARCOLACTICUM AC., STRAMONIUM, STRYCHNINUM,CHAMOMILLA, PHYTOLACCA, RUTA, SYMPHYTUM.	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-4759-1	openfda.package_ndc
ndc	product	55714-4759	openfda.product_ndc
ndc11	package	55714475901	derived:openfda.package_ndc
spl id		b5ab99d9-2e9f-5578-e053-2995a90a81b3	id
spl set id		9960c87f-f299-5d92-e053-2a95a90a7012	set_id
unii		11E6VI8VEG	openfda.unii
unii		XK4IUX8MNB	openfda.unii
unii		7E889U5RNN	openfda.unii
unii		269XH13919	openfda.unii
unii		H9Y79VD43J	openfda.unii
unii		O80TY208ZW	openfda.unii
unii		N94C2U587S	openfda.unii
unii		DL6OZ476V3	openfda.unii
unii		F9S9FFU82N	openfda.unii
unii		95IT3W8JZE	openfda.unii
unii		M9VVZ08EKQ	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		U0NQ8555JD	openfda.unii
unii		G6W4F0V8Z3	openfda.unii
unii		1W0775VX6E	openfda.unii
unii		G0R4UBI2ZZ	openfda.unii
unii		K73E24S6X9	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 out 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.