FDA.reportPublic FDA data

Camphor

Manufacturer
Chemco Corporation
Effective date
2020-06-23
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:18:46

Label at a glance#

ProductCamphor
Active ingredientISOPROPYL ALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

gel 4ozgel 4ozGel 5galGel 5galicegel 128ozicegel 128oz

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49283-331-042022-01-28C16284748780-1d6a99b39-aa89-a426-e053-dadaa90af4c249283-331-04
49283-331-052022-01-28C16284748780-1d6a99b39-aa89-a426-e053-dadaa90af4c249283-331-04
49283-331-282022-01-28C16284748780-1d6a99b39-aa89-a426-e053-dadaa90af4c249283-331-04

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49283-331-04Camphor118 mL in 1 BOTTLEGEL1184
49283-331-05Camphor18927 mL in 1 PAILGEL189274
49283-331-28Camphor3785 mL in 1 BOTTLEGEL37854

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49283-331CAMPHOR GEL [CHEMCO CORPORATION]4Legacy NDC, 3 package rows20200624_a6c9d626-208e-5b20-e053-2a95a90a3444.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49283-33149283-331-28, 49283-331-05, 49283-331-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ISOPROPYL ALCOHOLND2M416302ACTIB
EUCALYPTUS GLOBULUS LEAFS546YLW6E6IACT
WATER059QF0KO0RIACT
MENTHA ARVENSIS LEAF OIL1AEY1M553NIACT
POLYSORBATE 207T1F30V5YHIACT
OLETH-20YTH167I2AGIACT
MENTHOLL7T10EIP3AIACT
CARBOMER 9404Q93RCW27EIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
DIPROPYLENE GLYCOL MONOCAPRATE MONOCAPRYLATE5980W979ELIACT
METHYLPARABENA2I8C7HI9TIACT
DMDM HYDANTOINBYR0546TOWIACT
SODIUM HYDROXIDE55X04QC32IIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a8c22d89-fc87-5472-e053-2995a90a8841a6c9d626-208e-5b20-e053-2a95a90a34442020-06-23Exact identifier
spl id: a8c22d89-fc87-5472-e053-2995a90a8841
spl set id: a6c9d626-208e-5b20-e053-2a95a90a3444

Reported adverse events (FAERS/openFDA)#

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