terrasil Bruise and Pain Relief Maximum Strength

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: terrasil Bruise and Pain Relief Maximum Strength
Generic name: CAMPHOR, MENTHOL
Manufacturer: Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions
Product type: HUMAN OTC DRUG
SPL set ID: 240b231d-a8b2-c64c-e063-6394a90a7440
SPL ID: 240b231d-a8b3-c64c-e063-6394a90a7440
Version: 1
Effective date: 2024-10-09
Source export date: 2026-10-30
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/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:29:28

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		terrasil Bruise and Pain Relief Maximum Strength	openfda.brand_name
generic name		CAMPHOR, MENTHOL	openfda.generic_name
manufacturer name		Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions	openfda.manufacturer_name
ndc	package	24909-042-50	openfda.package_ndc
ndc	product	24909-042	openfda.product_ndc
ndc11	package	24909004250	derived:openfda.package_ndc
rxcui		1802734	openfda.rxcui
spl id		240b231d-a8b3-c64c-e063-6394a90a7440	id
spl set id		240b231d-a8b2-c64c-e063-6394a90a7440	set_id
unii		L7T10EIP3A	openfda.unii
unii		N20HL7Q941	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. Do not use on wounds or damaged skin. When using this product avoid contact with eyes or mucous membranes; do not bandage tightly or use with a heating pad. Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days symptoms clear up and occur again within a few days excessive skin irritation develops. If pregnant or breastfeeding , ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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