Label: GOOD NEIGHBOR PHARMACY ALOE VERA- lidocaine hydrochloride gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 July 22, 2015

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

  • Drug Facts

    Active Ingredients

    Lidocaine Hydrochloride 0.5%

    Pain Reliever

  • Temporary relief of pain and itching due to sunburn, minor burns, insect bites, cuts, scrapes

  • For external use only

    Do not use in large quantities, particularly over raw or blistered areas.

    When using this product

    • avoid contact with eyes.

    Rinse with water if contact occurs.

    Stop use and ask a doctor if

    • condition worsens

    or clear up and occur again within a few days.

    • if symptoms persist for more than 7 days.

  • Keep out of reach of children.

    If product is swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    • adults and children 2 years and older: apply to affected area not more than 3 - 4 times a day. • children under 2 years of age: consult a physician

  • INACTIVE INGREDIENT

    Aloe Barbadensis Leaf Juice, Carbomer, Diazolidinyl Urea, Disodium EDTA, FD&C Blue #1, FD&C Yellow #5, Glycerin, Isopropyl Alcohol (0.05% v/v), Menthol, Polysorbate 80, Propylene Glycol, Triethanolamine, Water.

  • SPL UNCLASSIFIED SECTION

    This product is not manufactured or distributed by Schering-Plough

    Healthcare Products, Inc., owner of the Solarcaine® trademark.

    Distributed By

    AmerisourceBergen

    1300 Morris Drive

    Chesterbrook, PA 19087

    Visit us at

    www.goodneighborpharmacy.com

  • Good Neighbor Pharmacy Aloe Vera Gel

    24385008334.jpg

  • INGREDIENTS AND APPEARANCE
    GOOD NEIGHBOR PHARMACY ALOE VERA 
    lidocaine hydrochloride gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24385-083
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE500 g  in 100000 mg
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    MENTHOL (UNII: L7T10EIP3A)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:24385-083-34500 mg in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34811/28/1988
    Labeler - Amerisourcebergen Drug Corporation (007914906)
    Establishment
    NameAddressID/FEIBusiness Operations
    Product Quest Mfg, LLC927768135manufacture(24385-083) , label(24385-083)