Walgreens Pain Relieving 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: Walgreens Pain Relieving Analgesic
Generic name: CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATE
Manufacturer: Walgreen Company
Product type: HUMAN OTC DRUG
SPL set ID: 3215a676-104c-43c3-aa36-b30d5b67799a
SPL ID: 523d49e7-1a59-47e8-8267-27e435c4a081
Version: 5
Effective date: 2024-10-30
Source export date: 2026-10-12
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:54:33

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		Walgreens Pain Relieving Analgesic	openfda.brand_name
generic name		CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATE	openfda.generic_name
manufacturer name		Walgreen Company	openfda.manufacturer_name
ndc	package	0363-1199-01	openfda.package_ndc
ndc	product	0363-1199	openfda.product_ndc
ndc11	package	00363119901	derived:openfda.package_ndc
rxcui		283083	openfda.rxcui
spl id		523d49e7-1a59-47e8-8267-27e435c4a081	id
spl set id		3215a676-104c-43c3-aa36-b30d5b67799a	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 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 breast feeding ask a health professional before use When using this product use only as directed do not swallow do not bandage tightly Stop use and consult a doctor if condition worsens or pain lasts 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.