Label: BABY OILOGIC SKIN AID DIAPER RASH- zinc oxide spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 7, 2024

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

  • Drug Facts

  • Active ingredient

    Zinc Oxide 15%

    Purpose

    Skin Protectant

  • Use(s)

    • Helps treat and prevent diaper rash
    • Protects minor skin irritation associated with diaper rash
    • Helps seal out wetness
  • Warnings

    For external use only.

    When using this product

    • avoid contact with eyes

    Stop use and ask a doctor if

    • condition lasts more than 7 days or clears up and occurs again within a few days.

    Keep out of reach of children.

    • If swallowed get medical help or contact a Poison Control Center right away.
    • Lock sprayer when not in use.
  • Directions

    • Shake well and unlock before each use.
    • Change wet and soiled diapers promptly, cleanse the diaper area, and allow to dry.
    • Spray product liberally as often as necessary with each diaper change, especially at bedtime or anytime when exposure to wet diapers may be prolonged.
    • Lock sprayer after use.
  • Inactive Ingredients:

    Acacia Senegal Gum, Calendula Officinalis Flower Extract, Caprylhydroxamic Acid, Caprylic/Capric Triglyceride, Caprylyl Glycol, Cellulose Gum, Coco-Caprylate/Caprate, Cocos Nucifera (Coconut) Oil, Glycerin, Lavandula Angustifolia (Lavender) Oil, Methyl Dihydroabietate, Microcrystalline Cellulose, Propanediol, Simmondsia Chinensis (Jojoba) Seed Oil, Tricaprylin, Water (Aqua), Xanthan Gum, Zinc Carbonate.

  • Other Information

    • Store between 59-87° F
  • Questions?

    1-888-645-6442 or www.oilogicbaby.com

  • package Labeling:

    Outer Label0Inner Label0

  • INGREDIENTS AND APPEARANCE
    BABY OILOGIC SKIN AID DIAPER RASH 
    zinc oxide spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79948-057
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION150 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ACACIA (UNII: 5C5403N26O)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    JOJOBA OIL (UNII: 724GKU717M)  
    TRICAPRILIN (UNII: 6P92858988)  
    WATER (UNII: 059QF0KO0R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ZINC CARBONATE (UNII: EQR32Y7H0M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79948-057-001 in 1 CARTON06/01/2024
    150.3 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01606/01/2024
    Labeler - Ignite Brands, LLC (079843577)