OHM Muscle and Joint Pain Relief 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: OHM Muscle and Joint Pain Relief Gel
Generic name: ARNICA, ACONITUM NAP, ARNICA, BELLADONNA, BELLIS, CALC FLUOR, CALC PHOS, CALENDULA, ECHINACEA PURP, HAMAMELIS, HYPERICUM, KALI MUR, LEDUM, MAG PHOS, RHUS TOX, RUTA, SYMPHYTUM.
Manufacturer: OHM PHARMA INC.
Product type: HUMAN OTC DRUG
SPL set ID: dec901c4-6a57-4151-8982-a9e256a48624
SPL ID: d44b6e78-253d-2edc-e053-2995a90a4b4d
Version: 4
Effective date: 2021-12-29
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 06:18:48

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 · 24 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		OHM Muscle and Joint Pain Relief Gel	openfda.brand_name
generic name		ARNICA, ACONITUM NAP, ARNICA, BELLADONNA, BELLIS, CALC FLUOR, CALC PHOS, CALENDULA, ECHINACEA PURP, HAMAMELIS, HYPERICUM, KALI MUR, LEDUM, MAG PHOS, RHUS TOX, RUTA, SYMPHYTUM.	openfda.generic_name
manufacturer name		OHM PHARMA INC.	openfda.manufacturer_name
ndc	package	66096-701-10	openfda.package_ndc
ndc	product	66096-701	openfda.product_ndc
ndc11	package	66096070110	derived:openfda.package_ndc
spl id		d44b6e78-253d-2edc-e053-2995a90a4b4d	id
spl set id		dec901c4-6a57-4151-8982-a9e256a48624	set_id
unii		877L01IZ0P	openfda.unii
unii		XK4IUX8MNB	openfda.unii
unii		O3B55K4YKI	openfda.unii
unii		O80TY208ZW	openfda.unii
unii		18E7415PXQ	openfda.unii
unii		2HU33I03UY	openfda.unii
unii		91D9GV0Z28	openfda.unii
unii		N94C2U587S	openfda.unii
unii		HF539G9L3Q	openfda.unii
unii		M9VVZ08EKQ	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		660YQ98I10	openfda.unii
unii		WQZ3G9PF0H	openfda.unii
unii		QI7G114Y98	openfda.unii
unii		U0NQ8555JD	openfda.unii
unii		T7S323PKJS	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 TOPICAL USE ONLY. DO NOT APPLY TO BROKEN SKIN. KEEP OUT OF THE REACH OF CHILDREN. IF PREGNANT OR BREAST - FEEDING, ask a health care professional before use. If symptoms worsen or persist for more than 5 days, discontinue use and contact a health care professional. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. Keep out of the reach of children.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.