CYBER CLEAN MOISTURIZING HAND SANITIZERSPRAY LEMON- alcohol hand sanitizer liquid CYBER CLEAN MOISTURIZING HAND SANITIZERSPRAY ORANGE BLOSSOM- alcohol hand sanitizer liquid CYBER CLEAN MOISTURIZING HAND SANITIZERSPRAY LAVENDER- alcohol hand sanitizer liquid CYBER CLEAN MOISTURIZING HAND SANITIZERSPRAY GRAPEFRUIT- alcohol hand sanitizer liquid CYBER CLEAN MOISTURIZING HAND SANITIZERSPRAY VANILLA- alcohol hand sanitizer liquid CYBER CLEAN MOISTURIZING HAND SANITIZERSPRAY EUCALYPTUS- alcohol hand sanitizer liquid

Cyber Clean Moisturizing Hand SanitizerSpray Eucalyptus by

Drug Labeling and Warnings

Cyber Clean Moisturizing Hand SanitizerSpray Eucalyptus by is a Otc medication manufactured, distributed, or labeled by JOKER AG, Guangzhou Berfly Cosmetic Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Cyber Clean Moisturizing Hand Sanitizer Spray Grapefruit
Cyber Clean Moisturizing Hand Sanitizer Spray Lemon
Cyber Clean Moisturizing Hand Sanitizer Spray Vanilla
Cyber Clean Moisturizing Hand Sanitizer Spray Orange Blossom
Cyber Clean Moisturizing Hand Sanitizer Spray Lavender
Cyber Clean Moisturizing Hand Sanitizer Spray Eucalyptus

Active Ingredient(s)

Alcohol 79% 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

• Massage into all areas for 30-40 seconds
• Ensure fingers, between fingers, thumbs, nails and nail beds, and wrist areas are massaged until liquid evaporates
• For best results: Do not wipe
• Do not rinse

Other information

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

Inactive ingredients

Cyber Clean Moisturizing Hand SanitizerSpray Grapefruit:

Water
Glycerol
Aloe barbadensis leaf extract
Propylene Glycol
FD&C Red 40
Tocopheryl acetate
Jojoba Oil

Cyber Clean Moisturizing Hand SanitizerSpray Lemon:

Water
Glycerol
Aloe barbadensis leaf extract
Propylene Glycol
FD&C Yellow 5
Tocopheryl acetate
Jojoba Oil

Cyber Clean Moisturizing Hand SanitizerSpray Vanilla:

Water
Glycerol
Aloe barbadensis leaf extract
Propylene Glycol
D&C Red 33
FD&C Yellow 5
FD&C Red 40
FD&C Blue 1
Tocopheryl acetate
Jojoba Oil

Cyber Clean Moisturizing Hand SanitizerSpray Orange Blossom:

Water
Glycerol
Aloe barbadensis leaf extract
Propylene Glycol
D&C Orange 4
Tocopheryl acetate
Jojoba Oil

Cyber Clean Moisturizing Hand SanitizerSpray Lavender:

Water
Glycerol
Aloe barbadensis leaf extract
Propylene Glycol
D&C Red 33
FD&C Blue 1
Tocopheryl acetate
Jojoba Oil

Cyber Clean Moisturizing Hand SanitizerSpray Eucalyptus:

Water
Glycerol
Aloe barbadensis leaf extract
Propylene Glycol
FD&C Yellow 5
FD&C Blue 1
Tocopheryl acetate
Jojoba Oil

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

CYBER CLEAN MOISTURIZING HAND SANITIZERSPRAY LEMON 
alcohol hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75757-124
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	79 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
JOJOBA OIL (UNII: 724GKU717M)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75757-124-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
2	NDC: 75757-124-02	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
3	NDC: 75757-124-03	175 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
4	NDC: 75757-124-04	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/02/2020

CYBER CLEAN MOISTURIZING HAND SANITIZERSPRAY ORANGE BLOSSOM 
alcohol hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75757-126
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	79 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)
JOJOBA OIL (UNII: 724GKU717M)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75757-126-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
2	NDC: 75757-126-02	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
3	NDC: 75757-126-03	175 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
4	NDC: 75757-126-04	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/02/2020

CYBER CLEAN MOISTURIZING HAND SANITIZERSPRAY LAVENDER 
alcohol hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75757-127
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	79 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
JOJOBA OIL (UNII: 724GKU717M)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75757-127-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
2	NDC: 75757-127-02	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
3	NDC: 75757-127-03	175 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
4	NDC: 75757-127-04	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/02/2020

CYBER CLEAN MOISTURIZING HAND SANITIZERSPRAY GRAPEFRUIT 
alcohol hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75757-123
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	79 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C RED NO. 40 (UNII: WZB9127XOA)
JOJOBA OIL (UNII: 724GKU717M)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75757-123-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
2	NDC: 75757-123-02	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
3	NDC: 75757-123-03	175 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
4	NDC: 75757-123-04	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/02/2020

CYBER CLEAN MOISTURIZING HAND SANITIZERSPRAY VANILLA 
alcohol hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75757-125
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	79 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
JOJOBA OIL (UNII: 724GKU717M)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75757-125-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
2	NDC: 75757-125-02	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
3	NDC: 75757-125-03	175 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
4	NDC: 75757-125-04	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/02/2020

CYBER CLEAN MOISTURIZING HAND SANITIZERSPRAY EUCALYPTUS 
alcohol hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75757-128
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	79 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
JOJOBA OIL (UNII: 724GKU717M)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75757-128-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
2	NDC: 75757-128-02	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
3	NDC: 75757-128-03	175 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020
4	NDC: 75757-128-04	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/02/2020

Labeler - JOKER AG (480850932)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Berfly Cosmetic Co., Ltd		553098664	manufacture(75757-123, 75757-124, 75757-125, 75757-126, 75757-127, 75757-128)