Meijer Ultra Strength Pain Relieving Topical Analgesic

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: Meijer Ultra Strength Pain Relieving Topical Analgesic
Generic name: CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATE
Manufacturer: Meijer Distribution, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 6319b019-8e17-4de1-b4e0-b402288a97d4
SPL ID: d22cd992-62af-4018-837a-a453e0c91077
Version: 4
Effective date: 2024-11-15
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:54:38

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Meijer Ultra Strength Pain Relieving Topical Analgesic	openfda.brand_name
generic name		CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATE	openfda.generic_name
manufacturer name		Meijer Distribution, Inc	openfda.manufacturer_name
ndc	package	79481-1220-1	openfda.package_ndc
ndc	product	79481-1220	openfda.product_ndc
ndc11	package	79481122001	derived:openfda.package_ndc
rxcui		283083	openfda.rxcui
spl id		d22cd992-62af-4018-837a-a453e0c91077	id
spl set id		6319b019-8e17-4de1-b4e0-b402288a97d4	set_id
unii		L7T10EIP3A	openfda.unii
unii		5TJD82A1ET	openfda.unii
unii		LAV5U5022Y	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. ALLERGY ALERT if prone to allergic reaction from aspirin or salicylates, consult a doctor before use. Avoid contact with the eyes and mucous membranes. Do not use for arthritis-like conditions in children under 12. Consult a doctor. with a heating pad on wounds or damaged skin If pregnant or breastfeeding ask a health professional before use. When using this product use only as directed do not swallow do not bandage tightly Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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