LILY HAND SANITIZER- alcohol spray LILY HAND SANITIZER GEL- alcohol gel

Lily Hand Sanitizer Gel by

Drug Labeling and Warnings

Lily 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)

Gel Inactive ingredients

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

Spray Inactive Ingredients

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

Spray Package Label - Principal Display Panel

120 mL NDC: 74164-001-12

250 mL NDC: 74164-001-25

500 mL NDC: 74164-001-50

Gel Package Label - Principal Display Panel

120 mL NDC: 74164-002-12

200 mL NDC: 74164-002-20

400 mL NDC: 74164-002-40

500 mL NDC: 74164-002-50

1.5 L NDC: 74164-002-15

INGREDIENTS AND APPEARANCE

LILY HAND SANITIZER 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74164-001
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)	0.75 mL  in 100 mL
TROLAMINE (UNII: 9O3K93S3TK)	0.15 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	2 mL  in 100 mL
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)	0.1 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	26 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74164-001-12	120 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/13/2020
2	NDC: 74164-001-25	250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/13/2020
3	NDC: 74164-001-50	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

LILY HAND SANITIZER GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74164-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
LAVENDER OIL (UNII: ZBP1YXW0H8)	0.15 mL  in 100 mL
TROLAMINE (UNII: 9O3K93S3TK)	0.15 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	2 mL  in 100 mL
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)	0.25 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	27.45 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74164-002-40	400 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
2	NDC: 74164-002-20	200 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
3	NDC: 74164-002-12	120 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
4	NDC: 74164-002-50	500 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/13/2020
5	NDC: 74164-002-15	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(74164-001, 74164-002)