ZIHUADICK PAIN RELIEVING (CAMPHOR MENTHOL METHYL SALICYLATE) LIQUID [WAH SING PHARMACEUTICAL LIMITED]

ZIHUADICK PAIN RELIEVING (CAMPHOR MENTHOL METHYL SALICYLATE) LIQUID [WAH SING PHARMACEUTICAL LIMITED]
PDF | XML

NDC 49969-002-01, 49969-002-50
Set ID e6a58a3e-8c6f-4dc0-ae5d-08a40f20ac27
Category HUMAN OTC DRUG LABEL
Packager Wah Sing Pharmaceutical Limited
Generic Name
Product Class
Product Number
Application Number PART348
  • Active Ingredients

    Camphor 3%

    Menthol 10%

    Methyl Salicylate 10%

  • Purpose

    External analgesic

    External analgesic

    External analgesic

  • Uses

    For the temporary relief of minor aches and pains of muscles and joints associated with:

    ■ simple backache ■ arthritis ■ strains ■ bruises ■ sprains

  • Warnings

    For external use only

    ■ Avoid getting into the eyes or on mucous membranes

    ■ Discontinue use if excessive irritation of the skin develops

  • When using this product

    ■ Do not apply to wound or damaged skin.

    ■ Do not bandage tightly

  • Stop use and ask a doctor if

    ■ Condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days

    ■ Pain persists for more than 10 days conditions

    ■ redness is present

    ■ Conditions affect children under 12 years of age

  • Keep out of reach of children

    to avoid accidental poisoning. If swallowed, get medical help or contact a poison control center right away.

  • Directions

    ■ Adults and children 12 years of age and older apply to affected area not more than 3 to 4 time daily

    ■ Apply liberally and gently rub into affected area

    ■ Children under 12 years of age, consult a doctor before using

    ■ Do not use otherwise than as directed

  • Inactive ingredients

    Alcohol, Eucalyptus oil, Glycerol, Water

  • Package Label

    image description

  • INGREDIENTS AND APPEARANCE
    ZIHUADICK  PAIN RELIEVING
    camphor menthol methyl salicylate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49969-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)3 g  in 100 mL
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10 g  in 100 mL
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE10 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49969-002-011 in 1 BOX
    1NDC:49969-002-5050 mL in 1 BOTTLE, WITH APPLICATOR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34812/30/2013
    Labeler - Wah Sing Pharmaceutical Limited (668844181)
    Establishment
    NameAddressID/FEIBusiness Operations
    Wah Sing Pharmaceutical Limited668844181manufacture(49969-002)

Related Drugs