Label: GERIGARD- zinc oxide ointment

  • NDC Code(s): 69771-050-04
  • Packager: Geri-Gentle Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 10, 2023

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  • Drug Facts

  • Active ingredient

    Zinc Oxide (1.8% w/w)

    Purpose

    Skin Prorectant

  • Uses:

    • Helps treat and prevent diaper rash.
    • Helps seal out wetness.
    • Dries the oozing and weeping of:
    • poison ivy 
    • poison oak 
    • poison sumac
  • Warnings:

    For external use only

    When using this product

    • Do not get into eyes

    Stop use nd ask a doctor if:

    • Condition worsens
    • Symptoms last more than 7 days or clear up and occur again in a few days, consult a physician

    Keep out of reach of children

    • If swallowed, get medical help or contact a Poison Control Center right away
  • Directions:

    • Apply liberally as needed
    • For diaper rash: 
    • change wet and soiled diapers promptly 
    • allow to dry
    • Apply ointment liberally with each diaper change
  • Other information:

    • Store at room temperature 15º - 30ºC (59º - 86ºF)
    • Avoid excessive heat
    • Contains color additives including FD&C Yellow No. 5 (Tartrazine).
  • Inactive ingredients:

    Aloe Vera Leaf, Alpha-Tocopherol, Ceteth-10, Cetostearyl Alcohol, Cetyl Alcohol, Cholecalciferol, Glycerin, Lanolin, Lavender, Methylparaben, Mineral Oil, Paraffin, Petrolatum, Phenoxyethanol, Polyethylene Glycol 6000, Polysorbate 60, Propylparaben Sodium, Steareth-20, Trolamine, Vitamin A, Water.

  • Package Labeling:

    geri

  • INGREDIENTS AND APPEARANCE
    GERIGARD 
    zinc oxide ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69771-050
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION18 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)  
    CETETH-10 (UNII: LF9X1PN3XJ)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LANOLIN (UNII: 7EV65EAW6H)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    PROPYLPARABEN SODIUM (UNII: 625NNB0G9N)  
    STEARETH-20 (UNII: L0Q8IK9E08)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    VITAMIN A (UNII: 81G40H8B0T)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69771-050-0424 in 1 CASE08/07/2018
    1113 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01608/07/2018
    Labeler - Geri-Gentle Corporation (080367686)
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