EXTRA STRENGTH SHINGLES CHICKENPOX RELIEF (LIDOCAINE HCL) GEL [RIDGE PROPERTIES]

EXTRA STRENGTH SHINGLES CHICKENPOX RELIEF (LIDOCAINE HCL) GEL [RIDGE PROPERTIES]
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NDC 69804-062-13, 69804-062-14, 69804-062-15, 69804-062-16
Set ID 4e400aef-05be-2aea-e054-00144ff88e88
Category HUMAN OTC DRUG LABEL
Packager ridge properties
Generic Name
Product Class Amide Local Anesthetic, Antiarrhythmic
Product Number
Application Number PART348
  • DOSAGE & ADMINISTRATION

    dosage and administration

  • WARNINGS

    warnings

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • PURPOSE

    purpose

  • INDICATIONS & USAGE

    indications and usage

  • ACTIVE INGREDIENT

    active ingredients

  • INACTIVE INGREDIENT

    inactive ingredients

  • PRINCIPAL DISPLAY PANEL

    package label

  • INGREDIENTS AND APPEARANCE
    EXTRA STRENGTH SHINGLES CHICKENPOX RELIEF 
    lidocaine hcl gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69804-062
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS40 mg  in 1000 mg
    Inactive Ingredients
    Ingredient NameStrength
    WITCH HAZEL (UNII: 101I4J0U34) 200 mg  in 1000 mg
    ACHILLEA MILLEFOLIUM OIL (UNII: 97P5D0WG43) 75 mg  in 1000 mg
    ALOE VERA WHOLE (UNII: KIZ4X2EHYX) 310 mg  in 1000 mg
    COPAIBA OIL (UNII: 64VX45Y68N) 75 mg  in 1000 mg
    FLAX SEED (UNII: 4110YT348C) 75 mg  in 1000 mg
    NUTMEG OIL (UNII: Z1CLM48948) 75 mg  in 1000 mg
    PIPER METHYSTICUM WHOLE (UNII: 3P306S300W) 150 mg  in 1000 mg
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69804-062-1314200 mg in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/01/2017
    2NDC:69804-062-1428500 mg in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/01/2017
    3NDC:69804-062-1556700 mg in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/01/2017
    4NDC:69804-062-16113400 mg in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/01/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34805/01/2017
    Labeler - ridge properties (029478762)
    Establishment
    NameAddressID/FEIBusiness Operations
    ridge properties029478762manufacture(69804-062)

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