Plantar Fasciitis Cream

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: Plantar Fasciitis Cream
Generic name: CAMPHOR
Manufacturer: SOLALIA LLC
Product type: HUMAN OTC DRUG
SPL set ID: 388f33c2-2bdf-ded8-e063-6294a90aeeac
SPL ID: 388f33c2-2be0-ded8-e063-6294a90aeeac
Version: 1
Effective date: 2025-06-27
Source export date: 2026-10-27
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/2c7d3f7bcea1543046130e07dcbaf7eea5fb0ce23f7faa6458d1c6d80c3fa0c3/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:42:11

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Plantar Fasciitis Cream	openfda.brand_name
generic name		CAMPHOR	openfda.generic_name
manufacturer name		SOLALIA LLC	openfda.manufacturer_name
ndc	package	85849-012-01	openfda.package_ndc
ndc	product	85849-012	openfda.product_ndc
ndc11	package	85849001201	derived:openfda.package_ndc
rxcui		1873621	openfda.rxcui
spl id		388f33c2-2be0-ded8-e063-6294a90aeeac	id
spl set id		388f33c2-2bdf-ded8-e063-6294a90aeeac	set_id
unii		213N3S8275	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

For external use, do not take orally or get into eyes Do not use on open wounds. if there are abnormalities such as skin rashes and allergies, do not scratch. Avoid contact with eyes and mucous membranes If you experience an allergic reaction, discontinue use and consult a physician If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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