DDM Camphor Spirit

Manufacturer
Discount Drug Mart | Pharma Nobis, LLC
Effective date
2023-12-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:05:07

Label at a glance#

ProductDDM Camphor Spirit
Active ingredientCAMPHOR (NATURAL)
Label structure12 sections

Dosage and administration

(dilute 3 parts olive oil and mix well) Adults and children 2 yrs. and older. apply to th affected area not more than 3 or 4 times daily. Children under 2 yrs of age: consult a doctor befre use.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION


Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Camphor 10%

Purpose

OTC - PURPOSE SECTION

Counterirritant

Use

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches, muscle and joint pain associated with arthritis, strains, brusies and simple backache.

Warnings

WARNINGS SECTION

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.

When using this product

OTC - WHEN USING SECTION

Do not bandage tightly.

Discontinue use and consult a doctor if

OTC - STOP USE SECTION

condition worsens, or if excesive irritation develops.

symptoms persit for more than 7 days, or clear up and occur again within a few days.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center right away. In case of eye contact, flush eyes with running water for 15 minutes, get medical attention.

Directions

DOSAGE & ADMINISTRATION SECTION

(dilute 3 parts olive oil and mix well)

Adults and children 2 yrs. and older. apply to th affected area not more than 3 or 4 times daily.

Children under 2 yrs of age: consult a doctor befre use.

Other Information

OTHER SAFETY INFORMATION

Flammable: Keep away from spark, heat and flame.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol 84%, Purified Water

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
204935camphor spirit 10 % Topical SolutionPSN4
204935camphor 100 MG/ML Topical SolutionSCD4
204935camphor 10 % Concentrate for Topical SolutionSY4
204935camphor spirit 10 % Topical SolutionSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53943-467-92DDM Camphor Spirit59 mL in 1 BOTTLE, PLASTICLIQUID594

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53943-467DDM CAMPHOR SPIRIT (CAMPHOR 10%) LIQUID [DISCOUNT DRUG MART]4Current NDC, Legacy NDC, 1 package rows20231221_5d56cbe6-4e48-79eb-e053-2a91aa0a74d3.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53943-46753943-467-92

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CAMPHOR (NATURAL)N20HL7Q941ACTIB
ALCOHOL3K9958V90MIACT

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
DDM Camphor SpiritCAMPHOR 10%Discount Drug Mart5d56cbe6-4e48-79eb-e053-2a91aa0a74d32023-12-20WarningsExact identifier
ndc (package): 53943-467-92
ndc (product): 53943-467
ndc11 (package): 53943046792
spl id: 0cf331fe-33c0-3343-e063-6394a90a1120
spl set id: 5d56cbe6-4e48-79eb-e053-2a91aa0a74d3

Reported adverse events (FAERS/openFDA)#

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