Germa Camphor 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: Germa Camphor Analgesic
Generic name: CAMPHOR 10%
Manufacturer: Germa Products, LLC
Product type: HUMAN OTC DRUG
SPL set ID: bf90a459-6ffa-5698-e053-2a95a90aa64d
SPL ID: 40d07529-3a18-c44d-e063-6394a90af1dc
Version: 5
Effective date: 2025-10-10
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:38:05

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		Germa Camphor Analgesic	openfda.brand_name
generic name		CAMPHOR 10%	openfda.generic_name
manufacturer name		Germa Products, LLC	openfda.manufacturer_name
ndc	package	73635-5809-2	openfda.package_ndc
ndc	product	73635-5809	openfda.product_ndc
ndc11	package	73635580902	derived:openfda.package_ndc
rxcui		418604	openfda.rxcui
spl id		40d07529-3a18-c44d-e063-6394a90af1dc	id
spl set id		bf90a459-6ffa-5698-e053-2a95a90aa64d	set_id
unii		5TJD82A1ET	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 children • on irritated skin • in or near eyes or mucous membranes • on wounds or damaged skin • if prone to allergic reaction from any of the ingredient • on large areas of the body. • if you are taking any other medication or drinking alcohol • if safety seal is torn, broken or missing.

Reported adverse events (FAERS/openFDA)#

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