Label: CALADRYL CLEAR- pramoxine hydrochloride and zinc acetate lotion

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated October 17, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredientsPurpose

    Pramoxine HCl 1%

    Topical analgesic

    Zinc acetate 0.1%

    Skin protectant
  • Uses

    • temporarily relieves pain and itching associated with:
      • rashes due to poison ivy, poison oak or poison sumac
      • insect bites
      • minor skin irritation
      • minor cuts
    • dries the oozing and weeping of poison ivy, poison oak and poison sumac
  • Warnings

    For external use only.

    When using this productdo not get into eyes

    Stop use and ask a doctor if

    • condition worsens or does not improve within 7 days
    • symptoms persist for more than 7 days or clear up and occur again within a few days

    Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • shake well before use
    • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
    • children under 2 years of age: ask a doctor
  • Other information

    • store at 20° to 25°C (68° to 77°F)
  • Inactive ingredients

    SD alcohol 38-B, camphor, citric acid, diazolidinyl urea, fragrance, glycerin, hypromellose, methylparaben, polysorbate 40, propylene glycol, propylparaben, purified water, sodium citrate

  • Questions/Comments

    call 1-800-321-4576

  • SPL UNCLASSIFIED SECTION

    Distributed by:Bausch Health US, LLC, Bridgewater, NJ 08807 USA

    © 2020 Bausch Health Companies Inc. or its affiliates

    Rev. 01/2020
    Made in Canada

  • PRINCIPAL DISPLAY PANEL - 177 mL Bottle Label

    Caladryl ®
    Clear ®
    Topical Analgesic ∙ Skin Protectant
    Lotion

    Drying Action PLUSItch Relief

    6 FL OZ (177 mL)

    label.jpg
  • INGREDIENTS AND APPEARANCE
    CALADRYL CLEAR 
    pramoxine hydrochloride and zinc acetate lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0187-5466
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 1 mL
    ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POLYSORBATE 40 (UNII: STI11B5A2X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0187-5466-06177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/16/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01408/16/2013
    Labeler - Bausch Health US, LLC (831922468)
    Establishment
    NameAddressID/FEIBusiness Operations
    Trillium Health Care Products Inc.255426306manufacture(0187-5466)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!