Camphor Ointment

Manufacturer
Germa Products, LLC
Effective date
2026-10-09
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
daily-update
Hydrated at
2026-10-13 04:05:07

Label at a glance#

ProductGerma Camphor Analgesic
Active ingredientCAMPHOR (SYNTHETIC)
Label structure12 sections

Indications and uses

Temporary relief of minor pain • Rheumatism • Muscular aches • Arthritis • Backache

Dosage and administration

Adults; 18 years of age and older, apply in affected area not more than 3 times daily.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Camphor 10%

Uses

OTC - WHEN USING SECTION

Temporary relief of minor pain • Rheumatism • Muscular aches • Arthritis • Backache

INDICATIONS & USAGE SECTION

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.

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Warnings

WARNINGS SECTION

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.

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding • ask a health professional before use.

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor • if condition worsens or cleans up and occurs again • if symptoms persist for more than 7 days or irritation or severe burning occurs.

Other Information

OTHER SAFETY INFORMATION

Store at controlled room temperature 15-30ºC (59-86ºF)

Directions

DOSAGE & ADMINISTRATION SECTION

Adults; 18 years of age and older, apply in affected area not more than 3 times daily.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Petrolatum

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Camphor OintmentCamphor Ointment

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130790933303025GTIN-13: 0790933303025
EAN-13: 0790933303025
GTIN-12: 790933303025
UPC-A: 790933303025
GTIN storage (14 digits): 00790933303025
Camphor.jpg

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73635-580973635-5809-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
WHITE PETROLATUMB6E5W8RQJ4IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52025-10-10full-release2026-06-01 01:38:40
42024-10-15full-release2026-06-01 00:25:52

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
40d07529-3a18-c44d-e063-6394a90af1dcbf90a459-6ffa-5698-e053-2a95a90aa64d2025-10-10WarningsExact identifier
spl set id: bf90a459-6ffa-5698-e053-2a95a90aa64d

Reported adverse events (FAERS/openFDA)#

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