BUBBLY SUDS ALOE VERA HAND SANITIZER- alcohol spray BUBBLY SUDS ALOE VERA HAND SANITIZER GEL- alcohol gel BUBBLY SUDS LAVENDER HAND SANITIZER- alcohol spray BUBBLY SUDS LAVENDER HAND SANITIZER GEL- alcohol gel

Bubbly Suds Lavender Hand Sanitizer Gel by

Drug Labeling and Warnings

Bubbly Suds Lavender Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by My Hao. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 70% 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)

Lavender Spray Inactive ingredients

Water (Aqua), Glycerin, Lavender Oil

Lavender Gel Inactive Ingredients

Water (Aqua), Glycerin, Lavender Oil

Aloe Spray Inactive Ingredients

Water (Aqua), Glycerin, Aloe Vera Extract

Aloe Gel Inactive Ingredients

Water (Aqua), Glycerin, Aloe Vera Extract

Lavender Spray Package Label - Principal Display Panel

120 mL NDC: 74164-003-12

250 mL NDC: 74164-003-25

500 mL NDC: 74164-003-50

Lavender Gel Package Label - Principal Display Panel

120 mL NDC: 74164-004-12

200 mL NDC: 74164-004-20

400 mL NDC: 74164-004-40

500 mL NDC: 74164-004-50

1.5 L NDC: 74164-004-15

Aloe Vera Spray Package Label - Principal Display Panel

120 mL NDC: 74164-005-12

250 mL NDC: 74164-005-25

500 mL NDC: 74164-005-50

Aloe Vera Gel Package Label - Principal Display Panel

120ml NDC: 74164-006-12

200mL NDC: 774164-006-20

400mL NDC: 774164-006-40

500mL NDC: 774164-006-50

1.5L NDC: 774164-006-15

INGREDIENTS AND APPEARANCE

BUBBLY SUDS ALOE VERA HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74164-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	71 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.01 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	2 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	26.99 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74164-005-12	120 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/13/2020
2	NDC: 74164-005-25	250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/13/2020
3	NDC: 74164-005-50	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/13/2020

BUBBLY SUDS ALOE VERA HAND SANITIZER GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74164-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	73 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.01 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	2 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	24.99 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74164-006-40	400 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
2	NDC: 74164-006-20	200 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
3	NDC: 74164-006-12	120 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
4	NDC: 74164-006-50	500 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
5	NDC: 74164-006-15	1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/13/2020

BUBBLY SUDS LAVENDER HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74164-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	71 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LAVENDER OIL (UNII: ZBP1YXW0H8)	0.01 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	2 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	26.99 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74164-003-12	120 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/13/2020
2	NDC: 74164-003-25	250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/13/2020
3	NDC: 74164-003-50	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/13/2020

BUBBLY SUDS LAVENDER HAND SANITIZER GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74164-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	73 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LAVENDER OIL (UNII: ZBP1YXW0H8)	0.01 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	2 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	24.99 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74164-004-40	400 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
2	NDC: 74164-004-20	200 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
3	NDC: 74164-004-12	120 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
4	NDC: 74164-004-50	500 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
5	NDC: 74164-004-15	1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/13/2020

Labeler - My Hao (555377964)

Establishment
Name	Address	ID/FEI	Business Operations
My Hao		555377964	manufacture(74164-003, 74164-004, 74164-005, 74164-006)