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

Drug Label Information

Updated October 10, 2024

If you are a consumer or patient please visit this version.

  • 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 DrugM01707/26/2012
    Labeler - DLC Laboratories, Inc. (093351930)
    Establishment
    NameAddressID/FEIBusiness Operations
    DLC Laboratories, Inc.093351930manufacture(24286-1521) , label(24286-1521)