Camphor Spirit

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: Camphor Spirit
Generic name: CAMPHOR 10%
Manufacturer: Pharma Nobis, LLC
Product type: HUMAN OTC DRUG
SPL set ID: e42fbe63-b01c-4f85-e053-2a95a90a5143
SPL ID: 0d6ccb8f-d9be-28e6-e063-6294a90a8a87
Version: 2
Effective date: 2023-12-26
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:19:05

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		Camphor Spirit	openfda.brand_name
generic name		CAMPHOR 10%	openfda.generic_name
manufacturer name		Pharma Nobis, LLC	openfda.manufacturer_name
ndc	package	82645-920-92	openfda.package_ndc
ndc	product	82645-920	openfda.product_ndc
ndc11	package	82645092092	derived:openfda.package_ndc
rxcui		204935	openfda.rxcui
spl id		0d6ccb8f-d9be-28e6-e063-6294a90a8a87	id
spl set id		e42fbe63-b01c-4f85-e053-2a95a90a5143	set_id
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 drink. If swallowed, immediately give 3 or 4 glases of water. Do not induce vomiting. If vomiting occurs, give fluids again. Do not give anything by mouth to an unconscious or convulsing person. Get medical attention immediately. Avoid contact with eyes or mucous membranes. Do not apply to irritated skin.

Reported adverse events (FAERS/openFDA)#

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