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 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 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.

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 Cream50 mL NDC: 82123-005

Propolis Nasal Plus

Nasal Spray Plus NDC: 82123-010

Propolis Nasal

Propolis Nasal NDC: 82123-009

SOS Cream

Sunscreen SPF50

Sunscreen SPF50 80 mL NDC: 82123-011

PROPOLIS NASAL PLUS
plus nasal liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:82123-010
Route of Administration	NASAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY)	OXYMETAZOLINE HYDROCHLORIDE	0.015 mg in 30 mL

Ingredient Name	Strength
Inactive Ingredients
EUCALYPTUS OIL (UNII: 2R04ONI662)
WATER (UNII: 059QF0KO0R)
SEA SALT (UNII: 87GE52P74G)
PROPOLIS WAX (UNII: 6Y8XYV2NOF)
GLYCERIN (UNII: PDC6A3C0OX)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:82123-010-31	1 in 1 BOX	10/03/2023
1	NDC:82123-010-30	30 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M012	10/03/2023

PROPOLIS NASAL
nasal liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:82123-009
Route of Administration	NASAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY)	OXYMETAZOLINE HYDROCHLORIDE	0.015 mg in 30 mL

Ingredient Name	Strength
Inactive Ingredients
EUCALYPTUS OIL (UNII: 2R04ONI662)
SEA SALT (UNII: 87GE52P74G)
GLYCERIN (UNII: PDC6A3C0OX)
PROPOLIS WAX (UNII: 6Y8XYV2NOF)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:82123-009-31	1 in 1 BOX	10/02/2023
1	NDC:82123-009-30	30 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M012	10/02/2023

SUNSCREEN SPF50
non nano zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:82123-011
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	12 mg in 80 mL

Ingredient Name	Strength
Inactive Ingredients
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
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:82123-011-81	1 in 1 TUBE	06/28/2021
1	NDC:82123-011-80	80 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	06/28/2021

SUNSCREEN FOR FACE SPF50
non nano zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:82123-013
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	6 mg in 40 mL

Ingredient Name	Strength
Inactive Ingredients
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
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:82123-013-41	1 in 1 TUBE	06/28/2021
1	NDC:82123-013-40	40 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	06/28/2021

AFTERSUN
non nano zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:82123-004
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	1.6 mg in 80 mL

Ingredient Name	Strength
Inactive Ingredients
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
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:82123-004-81	1 in 1 TUBE	06/28/2021
1	NDC:82123-004-80	80 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	06/28/2021

DIAPER RASH CREAM
non nano zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:82123-005
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	11 mg in 50 mg

Ingredient Name	Strength
Inactive Ingredients
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
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:82123-005-51	1 in 1 TUBE	06/28/2021
1	NDC:82123-005-50	50 mg in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M016	06/28/2021

SUNSCREEN FOR KIDS SPF50
non nano zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:82123-012
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	17.6 mg in 80 mg

Ingredient Name	Strength
Inactive Ingredients
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
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:82123-012-81	1 in 1 TUBE	06/28/2021
1	NDC:82123-012-80	80 mg in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	06/28/2021

S.O.S CREAM INTENSIVE MOISTURIZING SKIN PROTECTANT
non nano zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:82123-007
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.6 mg in 15 mL

Ingredient Name	Strength
Inactive Ingredients
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
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:82123-007-16	1 in 1 BOX	11/11/2021
1	NDC:82123-007-15	15 mL in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M016	11/11/2021

ACNE CONTROL SERUM
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:82123-008
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.15 mg in 30 mL

Ingredient Name	Strength
Inactive Ingredients
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
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:82123-008-31	1 in 1 BOX	10/11/2023
1	NDC:82123-008-30	30 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	09/29/2023

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)

Name	Address	ID/FEI	Business Operations
Establishment
SBS BILIMSEL BIO COZUMLER SANAYI VE TICARET ANONIM SIRKETI PINAR SUBESI		533166749	manufacture(82123-012, 82123-013, 82123-011, 82123-004, 82123-005, 82123-007, 82123-008, 82123-009, 82123-010)