Label: DE LA CRUZ CAMPHOR- camphor ointment

  • NDC Code(s): 24286-1521-2, 24286-1521-5
  • Packager: DLC Laboratories, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated March 23, 2021

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  • 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

  • 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

    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
  • INGREDIENTS AND APPEARANCE
    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 not finalpart34807/26/2012
    Labeler - DLC Laboratories, Inc. (093351930)
    Establishment
    NameAddressID/FEIBusiness Operations
    DLC Laboratories, Inc.093351930MANUFACTURE(24286-1521) , LABEL(24286-1521)
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