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

Acne Control Serum by

Drug Labeling and Warnings

Acne Control Serum by is a Otc medication manufactured, distributed, or labeled by SBS BILIMSEL BIO COZUMLER SANAYI VE TICARET ANONIM SIRKETI PINAR SUBESI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

Sunscreen for kids SPF50

Sunscreen for face SPF50

Aftersun

Diaper Rash Cream

Diaper Rash Cream50 mL NDC: 82123-005

Propolis Nasal Plus

Propolis Nasal

SOS Cream

SOS Cream

Sunscreen SPF50

INGREDIENTS AND APPEARANCE

PROPOLIS NASAL PLUS 
plus nasal liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82123-021
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY)	OXYMETAZOLINE HYDROCHLORIDE	15.21 mg  in 30 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82123-021-31	1 in 1 BOX	10/03/2023
1	NDC: 82123-021-30	30 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

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

PROPOLIS NASAL 
nasal liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82123-020
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OXYMETAZOLINE HYDROCHLORIDE (UNII: K89MJ0S5VY) (OXYMETAZOLINE - UNII:8VLN5B44ZY)	OXYMETAZOLINE HYDROCHLORIDE	15.21 mg  in 30 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82123-020-31	1 in 1 BOX	10/02/2023
1	NDC: 82123-020-30	30 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
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: 82123-014
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	18.9 g  in 80 mL

Inactive Ingredients
Ingredient Name	Strength
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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82123-014-81	1 in 1 TUBE	06/28/2021
1	NDC: 82123-014-80	80 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
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: 82123-016
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	10.4 g  in 40 mL

Inactive Ingredients
Ingredient Name	Strength
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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82123-016-41	1 in 1 TUBE	06/28/2021
1	NDC: 82123-016-40	40 mL in 1 TUBE; Type 0: Not a Combination Product

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

AFTERSUN 
non nano zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82123-023
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	1.55 g  in 80 mL

Inactive Ingredients
Ingredient Name	Strength
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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82123-023-81	1 in 1 TUBE	06/28/2021
1	NDC: 82123-023-80	80 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
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: 82123-022
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	11.55 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82123-022-51	1 in 1 TUBE	06/28/2021
1	NDC: 82123-022-50	50 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
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: 82123-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	21.2 g  in 80 mL

Inactive Ingredients
Ingredient Name	Strength
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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82123-015-81	1 in 1 TUBE	06/28/2021
1	NDC: 82123-015-80	80 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
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: 82123-018
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.57 g  in 15 mL

Inactive Ingredients
Ingredient Name	Strength
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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82123-018-16	1 in 1 BOX	11/11/2021
1	NDC: 82123-018-15	15 mL in 1 CONTAINER; Type 0: Not a Combination Product

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

ACNE CONTROL SERUM 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82123-019
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.14 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82123-019-31	1 in 1 BOX	10/11/2023
1	NDC: 82123-019-30	30 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
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)

Establishment
Name	Address	ID/FEI	Business Operations
SBS BILIMSEL BIO COZUMLER SANAYI VE TICARET ANONIM SIRKETI PINAR SUBESI		533166749	manufacture(82123-014, 82123-015, 82123-016, 82123-023, 82123-018, 82123-019, 82123-020, 82123-021, 82123-022)