CAMPHOR Ointment 11%

Manufacturer
DLC Laboratories, Inc.
Effective date
2024-10-10
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 00:24:14

Label at a glance#

ProductDe La Cruz Camphor
Active ingredientCAMPHOR (SYNTHETIC)
Label structure12 sections

Indications and uses

for the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains

Dosage and administration

adults and children 2 years of age or older, apply to affected area not more than 3 to 4 times daily children under 2 years of age: consult a doctor

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Camphor, USP 11%

Purpose

OTC - PURPOSE SECTION

External analgesic

Uses

INDICATIONS & USAGE SECTION

for the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes or mucous membranes

do not apply to wounds or damaged skin

do not bandage tightly or use with a heating pad

Stop use and consult a doctor if

OTC - STOP USE SECTION

condition worsens or if symptoms persist for more than 7 days

symptoms clear up and occur again within a few days.

excessive skin irritation develops

If pregnant or breastfeeding,

PREGNANCY SECTION

consult a doctor before use.

KEEP OUT OF THE REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 2 years of age or older, apply to affected area not more than 3 to 4 times daily

children under 2 years of age: consult a doctor

Inactive ingredient

INACTIVE INGREDIENT SECTION

polyethylene glycol

SPL UNCLASSIFIED SECTION

De La Cruz

CAMPHOR
Ointment 11%

Pain relieving rub

2.5 OZ (70.9g)


FAST, PENETRATING RELIEF FOR:

Muscle and joint pain

Backaches and arthritis

Strains and sprains

Itching


NON-IRRITATING

WATER WASHABLE

NO PARABENS OR ARTIFICIAL FRAGRANCES OR COLORS

Manufactured by:

De La Cruz Products

A Division of DLC Laboratories, Inc.

Paramount, CA 90723 USA

Questions: 1-800-858-3889

www.dlclabs.com (c) DLC

PRINCIPAL DISPLAY PANEL - 70.9 g Jar Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

De La Cruz ®

Clinically Tested*

CAMPHOR
OINTMENT 11%

Pain Relieving Rub

2.5 OZ (70.9 g)

Principal Display Panel - 70.9 g Jar Label
Principal Display Panel - 70.9 g Jar Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1090457camphor 11 % Topical OintmentPSN8
1090457camphor 0.11 MG/MG Topical OintmentSCD8
1090457camphor 11 % Topical OintmentSY8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
24286-1521-2De La Cruz Camphor70.9 g in 1 JAROINTMENT70.98
24286-1521-5De La Cruz Camphor155.9 g in 1 JAROINTMENT155.98

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24286-1521DE LA CRUZ CAMPHOR (CAMPHOR) OINTMENT [DLC LABORATORIES, INC.]8Current NDC, Legacy NDC, 2 package rows20241012_62359237-de2d-4497-bfd6-36991cfc8acf.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (SYNTHETIC)ACTIVE INGREDIENT5TJD82A1ET5
CAMPHOR (SYNTHETIC)ACTIVE MOIETY5TJD82A1ET5
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1A5

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
24286-152124286-1521-2, 24286-1521-5

Ingredients#

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

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

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
De La Cruz CamphorCAMPHORDLC Laboratories, Inc.62359237-de2d-4497-bfd6-36991cfc8acf2024-10-10WarningsExact identifier
ndc (package): 24286-1521-5
ndc (package): 24286-1521-2
ndc (product): 24286-1521
ndc11 (package): 24286152105
ndc11 (package): 24286152102
spl id: 2425f49f-ade6-5178-e063-6294a90adfac
spl set id: 62359237-de2d-4497-bfd6-36991cfc8acf

Reported adverse events (FAERS/openFDA)#

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