Label: WELL AT WALGREENS ANTI-ITCH MAXIMUM STRENGTH- benzocaine and resorcinol cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 January 24, 2018

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredients

    Benzocaine 20%

    Resorcinol 3%

  • Purpose

    External Analgesic

    External Analgesic

  • Use

    • Temporarily relieves itching
  • Warnings

    For external use only

    When using this product avoid contact with eyes

    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. Also, do not use if you have an unusual or abnormal vaginal discharge except under the supervision of a physician.

    Do not apply over large areas of the body

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

  • Directions

    adults and children 12 years and older

    apply a fingertip amount (approximately 1-inch strip) to affected area not more than 3 to 4 times daily

    children under 12 years

    consult a doctor

  • Other information

    store at 20°-25°C (68°-77°F)

  • Inactive ingredients

    aloe vera gel, carbomer, cetyl alcohol, disodium EDTA, fragrance, glyceryl stearate, isopropyl myristate, isopropyl palmitate, lanolin, methyl-4 hydroxybenzoate, mineral oil, PEG-100 stearate, propylene glycol, purified water, stearic acid corn oil, stearyl alcohol, triethanolamine, vitamin A, E & D

  • Principal display panel - 28 g Carton Label

    Well at Walgreens

    WALGREENS PHARMACIST RECOMMENDED

    NEW

    MAXIMUM STRENGTH

    Anti-Itch Cream

    Pain Relieving Cream

    • Instantly soothes & relieves external itching & burning
    • Soothes irritated skin with aloe
    • Helps prevent further irritation
    • Fresh, clean scent

    Compared to Vaglsil® Maximum Strength active ingredients‡‡

    Relieves vaginal itching.

    NDC 76466-500-04

    Well at Walgreens

    WALGREENS PHARMACIST RECOMMENDED

    MAXIMUM STRENGTH

    Anti-Itch Cream

    Pain Relieving Cream

    NET WT 1 OZ (28 g)

    Principal display panel - 28 g Carton Label
  • Principal display panel - 28 g Tube Label

    NDC 76466-500-04

    Well at Walgreens

    WALGREENS PHARMACIST RECOMMENDED

    MAXIMUM STRENGTH

    Anti-Itch Cream

    Pain Relieving Cream

    NET WT 1 OZ (28 g)

    Principal display panel - 28 g Tube Label
  • INGREDIENTS AND APPEARANCE
    WELL AT WALGREENS ANTI-ITCH   MAXIMUM STRENGTH
    benzocaine and resorcinol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76466-500
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE200 mg  in 1 g
    RESORCINOL (UNII: YUL4LO94HK) (RESORCINOL - UNII:YUL4LO94HK) RESORCINOL30 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    Aloe Vera Leaf (UNII: ZY81Z83H0X)  
    Carbomer Copolymer Type B (Allyl Pentaerythritol Crosslinked) (UNII: 809Y72KV36)  
    Cetyl Alcohol (UNII: 936JST6JCN)  
    Edetate Disodium (UNII: 7FLD91C86K)  
    Glyceryl Monostearate (UNII: 230OU9XXE4)  
    Isopropyl Myristate (UNII: 0RE8K4LNJS)  
    Isopropyl Palmitate (UNII: 8CRQ2TH63M)  
    Lanolin (UNII: 7EV65EAW6H)  
    Potassium Methylparaben (UNII: M64U971IB0)  
    Mineral Oil (UNII: T5L8T28FGP)  
    PEG-100 Stearate (UNII: YD01N1999R)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Water (UNII: 059QF0KO0R)  
    Stearic Acid (UNII: 4ELV7Z65AP)  
    Stearyl Alcohol (UNII: 2KR89I4H1Y)  
    Trolamine (UNII: 9O3K93S3TK)  
    Vitamin A (UNII: 81G40H8B0T)  
    Vitamin D (UNII: 9VU1KI44GP)  
    .Alpha.-Tocopherol (UNII: H4N855PNZ1)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76466-500-041 in 1 CARTON05/19/2014
    128 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34605/19/2014
    Labeler - SCI International (114220648)
    Establishment
    NameAddressID/FEIBusiness Operations
    Natural Essentials947484713MANUFACTURE(76466-500)