DE LA CRUZ CAMPHOR- camphor ointment 
DLC Laboratories, Inc.

----------

CAMPHOR Ointment 11%

Active Ingredient

Camphor, USP 11%

Purpose

External analgesic

Uses

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

Warnings

For external use only

When using this product

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

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,

consult a doctor before use.

KEEP OUT OF THE REACH OF CHILDREN.

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

Directions

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

polyethylene glycol

Questions?

1-800-858-3889 or www.dlclabs.com

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

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
DE LA CRUZ CAMPHOR 
camphor ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1521
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)11 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24286-1521-270.9 g in 1 JAR; Type 0: Not a Combination Product07/26/2012
2NDC:24286-1521-5155.9 g in 1 JAR; Type 0: Not a Combination Product03/10/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01707/26/2012
Labeler - DLC Laboratories, Inc. (093351930)
Establishment
NameAddressID/FEIBusiness Operations
DLC Laboratories, Inc.093351930manufacture(24286-1521) , label(24286-1521)

Revised: 10/2024
Document Id: 2425f49f-ade6-5178-e063-6294a90adfac
Set id: 62359237-de2d-4497-bfd6-36991cfc8acf
Version: 8
Effective Time: 20241010
 
DLC Laboratories, Inc.