Label: PROPOLIS NASAL PLUS- plus nasal liquid
PROPOLIS NASAL- nasal liquid
SUNSCREEN SPF50- non nano zinc oxide cream
SUNSCREEN FOR FACE SPF50- non nano zinc oxide cream
AFTERSUN- non nano zinc oxide cream
DIAPER RASH CREAM- non nano zinc oxide cream
SUNSCREEN FOR KIDS SPF50- non nano zinc oxide cream
S.O.S CREAM INTENSIVE MOISTURIZING SKIN PROTECTANT- non nano zinc oxide cream
ACNE CONTROL SERUM- salicylic acid liquid

  • NDC Code(s): 82123-004-80, 82123-004-81, 82123-005-50, 82123-005-51, view more
    82123-007-15, 82123-007-16, 82123-008-30, 82123-008-31, 82123-009-30, 82123-009-31, 82123-010-30, 82123-010-31, 82123-011-80, 82123-011-81, 82123-012-80, 82123-012-81, 82123-013-40, 82123-013-41
  • Packager: SBS BILIMSEL BIO COZUMLER SANAYI VE TICARET ANONIM SIRKETI PINAR SUBESI
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 9, 2023

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

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  • Active Ingredient(s)

    Alcohol 80% v/v. Purpose: Antiseptic

  • Purpose

    Antiseptic, Hand Sanitizer

  • Use

    Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Warnings

    For external use only. Flammable. Keep away from heat or flame

  • Do not use

    • in children less than 2 months of age
    • on open skin wounds
  • WHEN USING

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    • Place enough product on hands to cover all surfaces. Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Other information

    • Store between 15-30C (59-86F)
    • Avoid freezing and excessive heat above 40C (104F)
  • Inactive Ingredients

  • Acne Control Serum

    30 ml NDC:​ 82123-009 Acne Control Serum

  • Sunscreen for kids SPF50

    Sunscreen for kids SPF50 80 mL NDC: 82123-012

  • Sunscreen for face SPF50

    Sunscreen for face SPF50 40 mL NDC: 82123-013

  • Aftersun

    AfterSun 80 mL NDC: 82123-004

  • Diaper Rash Cream

    Diaper Rash CreamDiaper Rash Cream50 mL NDC: 82123-005

  • Propolis Nasal Plus

    Nasal Spray Plus NDC: 82123-010

  • Propolis Nasal

    Propolis Nasal NDC: 82123-009

  • SOS Cream

    SOS CreamSOS Cream

  • Sunscreen SPF50

    Sunscreen SPF50 80 mL NDC: 82123-011

  • INGREDIENTS AND APPEARANCE
    PROPOLIS NASAL PLUS 
    plus nasal liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82123-010
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE0.015 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    WATER (UNII: 059QF0KO0R)  
    SEA SALT (UNII: 87GE52P74G)  
    PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82123-010-311 in 1 BOX10/03/2023
    1NDC:82123-010-3030 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01210/03/2023
    PROPOLIS NASAL 
    nasal liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82123-009
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY) OXYMETAZOLINE HYDROCHLORIDE0.015 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    SEA SALT (UNII: 87GE52P74G)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82123-009-311 in 1 BOX10/02/2023
    1NDC:82123-009-3030 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01210/02/2023
    SUNSCREEN SPF50 
    non nano zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82123-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE12 mg  in 80 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU)  
    JOJOBA OIL (UNII: 724GKU717M)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
    MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ARGAN OIL (UNII: 4V59G5UW9X)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)  
    GLYCERYL CITRATE (UNII: 4987GT719I)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82123-011-811 in 1 TUBE06/28/2021
    1NDC:82123-011-8080 mL in 1 TUBE; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02006/28/2021
    SUNSCREEN FOR FACE SPF50 
    non nano zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82123-013
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE6 mg  in 40 mL
    Inactive Ingredients
    Ingredient NameStrength
    COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
    OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLES (UNII: XO45V955LT)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU)  
    MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)  
    GLYCERYL CITRATE (UNII: 4987GT719I)  
    PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)  
    ARGAN OIL (UNII: 4V59G5UW9X)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82123-013-411 in 1 TUBE06/28/2021
    1NDC:82123-013-4040 mL in 1 TUBE; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02006/28/2021
    AFTERSUN 
    non nano zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82123-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE1.6 mg  in 80 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
    SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)  
    PHYSALIS ANGULATA (UNII: W4TKW9D5GG)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERYL CITRATE (UNII: 4987GT719I)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    WATER (UNII: 059QF0KO0R)  
    BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU)  
    COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
    SESAME OIL (UNII: QX10HYY4QV)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ARGAN OIL (UNII: 4V59G5UW9X)  
    MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82123-004-811 in 1 TUBE06/28/2021
    1NDC:82123-004-8080 mL in 1 TUBE; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02006/28/2021
    DIAPER RASH CREAM 
    non nano zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82123-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE11 mg  in 50 mg
    Inactive Ingredients
    Ingredient NameStrength
    BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU)  
    HYDROLYZED JOJOBA ESTERS (POTASSIUM SALTS) (UNII: CH428W5O62)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    POLYGLYCERYL-3 OLEATE (UNII: XRQ165498B)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)  
    POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)  
    CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    JOJOBA OIL (UNII: 724GKU717M)  
    HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)  
    POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)  
    POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)  
    PALM OIL (UNII: 5QUO05548Z)  
    PALM KERNEL OIL (UNII: B0S90M0233)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    CANOLA OIL (UNII: 331KBJ17RK)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82123-005-511 in 1 TUBE06/28/2021
    1NDC:82123-005-5050 mg in 1 TUBE; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01606/28/2021
    SUNSCREEN FOR KIDS SPF50 
    non nano zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82123-012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE17.6 mg  in 80 mg
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I)  
    PALM KERNEL OIL (UNII: B0S90M0233)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    CANOLA OIL (UNII: 331KBJ17RK)  
    WATER (UNII: 059QF0KO0R)  
    COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
    BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU)  
    ARGAN OIL (UNII: 4V59G5UW9X)  
    GLYCERYL CITRATE (UNII: 4987GT719I)  
    PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PALM OIL (UNII: 5QUO05548Z)  
    SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82123-012-811 in 1 TUBE06/28/2021
    1NDC:82123-012-8080 mg in 1 TUBE; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02006/28/2021
    S.O.S CREAM INTENSIVE MOISTURIZING SKIN PROTECTANT 
    non nano zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82123-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.6 mg  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    HONEY (UNII: Y9H1V576FH)  
    PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
    BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLES (UNII: XO45V955LT)  
    WATER (UNII: 059QF0KO0R)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    ROYAL JELLY (UNII: L497I37F0C)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82123-007-161 in 1 BOX11/11/2021
    1NDC:82123-007-1515 mL in 1 CONTAINER; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01611/11/2021
    ACNE CONTROL SERUM 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82123-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.15 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    APIS MELLIFERA VENOM (UNII: 76013O881M)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    BEET (UNII: N487KM8COK)  
    CAPRYLIC ACID (UNII: OBL58JN025)  
    ROSA MULTIFLORA FRUIT (UNII: EZ5DSL4T27)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    ACTINIDIA POLYGAMA FRUIT (UNII: CJA97047JF)  
    XYLITOL (UNII: VCQ006KQ1E)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82123-008-311 in 1 BOX10/11/2023
    1NDC:82123-008-3030 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00609/29/2023
    Labeler - SBS BILIMSEL BIO COZUMLER SANAYI VE TICARET ANONIM SIRKETI PINAR SUBESI (533166749)
    Registrant - SBS BILIMSEL BIO COZUMLER SANAYI VE TICARET ANONIM SIRKETI PINAR SUBESI (533166749)
    Establishment
    NameAddressID/FEIBusiness Operations
    SBS BILIMSEL BIO COZUMLER SANAYI VE TICARET ANONIM SIRKETI PINAR SUBESI533166749manufacture(82123-012, 82123-013, 82123-011, 82123-004, 82123-005, 82123-007, 82123-008, 82123-009, 82123-010)
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