Ultra Strength Pain Relief Balm

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: Ultra Strength Pain Relief Balm
Generic name: CAMPHOR, MENTHOL
Manufacturer: ALAINA HEALTHCARE PRIVATE LIMITED
Product type: HUMAN OTC DRUG
SPL set ID: 80779d1f-0c2a-4ae5-9ed7-eb6877f734ba
SPL ID: 4583ba32-cb31-6fdf-e063-6394a90a6803
Version: 4
Effective date: 2025-12-09
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 05:14:50

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Ultra Strength Pain Relief Balm	openfda.brand_name
generic name		CAMPHOR, MENTHOL	openfda.generic_name
manufacturer name		ALAINA HEALTHCARE PRIVATE LIMITED	openfda.manufacturer_name
ndc	package	73492-711-18	openfda.package_ndc
ndc	product	73492-711	openfda.product_ndc
ndc11	package	73492071118	derived:openfda.package_ndc
rxcui		1089847	openfda.rxcui
spl id		4583ba32-cb31-6fdf-e063-6394a90a6803	id
spl set id		80779d1f-0c2a-4ae5-9ed7-eb6877f734ba	set_id
unii		L7T10EIP3A	openfda.unii
unii		5TJD82A1ET	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. When using this product Use only as directed. avoid contact with eyes and mucous membranes. do not apply to wounds, damaged or irritated skin. do not bandage or cover with wrap or use heating pad. do not use 1 hour prior to bathing or within 30 minutes after bathing. Stop use and ask a doctor if condition worsens. severe skin irritation occurs. pain persists for more than 7 days. pain clears up and then recurs a few days later. If pregnant or breast-feeding, or if you have sensitive skin, ask a healthcare professional before use.

Reported adverse events (FAERS/openFDA)#

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