BUBBLY SUDS HAND SANITIZER GEL ALOE VERA GREEN- alcohol gel BUBBLY SUDS HAND SANITIZER GEL LAVENDER DREAM- alcohol gel

Bubbly Suds Hand Sanitizer Gel by

Drug Labeling and Warnings

Bubbly Suds 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 Gel Inactive Ingredients

Water (Aqua), Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Fragrance (Lavender Oil).

Aloe Gel Inactive Ingredients

Water (Aqua), Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Fragrance (Aloe Vera Extract).

Lavender Gel Package Label - Principal Display Panel

60ml NDC: 74164-007-60

100ml NDC: 74164-007-10

120ml NDC: 74164-007-12

200ml NDC: 74164-007-20

300ml NDC: 74164-007-30

500ml NDC: 74164-007-50

1000ml NDC: 74164-007-11

1500ml NDC: 74164-007-15

2000ml NDC: 74164-007-22

4000ml NDC: 74164-007-44

5000ml NDC: 74164-007-55

Aloe Vera Gel Package Label - Principal Display Panel

60ml NDC: 74164-008-60

100ml NDC: 74164-008-10

120ml NDC: 74164-008-12

200ml NDC: 74164-008-20

300ml NDC: 74164-008-30

500ml NDC: 74164-008-50

1000ml NDC: 74164-008-11

1500ml NDC: 74164-008-15

2000ml NDC: 74164-008-22

4000ml NDC: 74164-008-44

5000ml NDC: 74164-008-55

INGREDIENTS AND APPEARANCE

BUBBLY SUDS HAND SANITIZER GEL  ALOE VERA GREEN
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74164-008
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
TROLAMINE (UNII: 9O3K93S3TK)	0.07 mL  in 100 mL
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)	0.25 mL  in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.01 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	2 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	24.67 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74164-008-12	120 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
2	NDC: 74164-008-10	100 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
3	NDC: 74164-008-60	60 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
4	NDC: 74164-008-30	300 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
5	NDC: 74164-008-20	200 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
6	NDC: 74164-008-50	500 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
7	NDC: 74164-008-11	1000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
8	NDC: 74164-008-15	1500 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
9	NDC: 74164-008-22	2000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
10	NDC: 74164-008-44	4000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
11	NDC: 74164-008-55	5000 mL in 1 BOTTLE, DISPENSING; 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 HAND SANITIZER GEL  LAVENDER DREAM
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74164-007
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
TROLAMINE (UNII: 9O3K93S3TK)	0.07 mL  in 100 mL
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)	0.25 mL  in 100 mL
LAVENDER OIL (UNII: ZBP1YXW0H8)	0.01 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	2 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	24.67 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74164-007-12	120 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
2	NDC: 74164-007-10	100 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
3	NDC: 74164-007-60	60 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
4	NDC: 74164-007-30	300 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
5	NDC: 74164-007-20	200 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
6	NDC: 74164-007-50	500 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
7	NDC: 74164-007-11	1000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
8	NDC: 74164-007-15	1500 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
9	NDC: 74164-007-22	2000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
10	NDC: 74164-007-44	4000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
11	NDC: 74164-007-55	5000 mL in 1 BOTTLE, DISPENSING; 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(74164-007, 74164-008)