LILKOI HAND SANITIZER- ethyl alcohol spray

lilkoi Hand Sanitizer by

Drug Labeling and Warnings

lilkoi Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by D-Time Limited Liability Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 80%

Purpose

Antiseptic skin cleanser

Uses

For personal hand hygiene to help prevent the spread of bacteria.

Warnings

For external use only.

Flammable. Keep away from open flame and sources of heat.

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and consult a healthcare professional if irritation develops.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.If swallowed, contact a Poison Control Center or get medical help right away.

Directions

Adults and children over 2 years:   For occasional and personal domestic use   Supervise children when they use this product ∙ Spray onto hands and rub thoroughly for at least 30 seconds. Allow to dry.

Other information

Store at 68° to 70° F (20° to 25° C).

May discolor certain fabrics or surfaces.

Questions? 1-844-800-6858

Inactive ingredients

Water, Glycerin, Sweet almond oil, Lavender Flower Oil, Hydrogen Peroxide, Sodium pyruvate.

Lilkoi hand sanitizer

INGREDIENTS AND APPEARANCE

LILKOI HAND SANITIZER 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75306-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALMOND OIL (UNII: 66YXD4DKO9)
LAVENDER OIL (UNII: ZBP1YXW0H8)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
SODIUM PYRUVATE (UNII: POD38AIF08)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75306-007-17	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020
2	NDC: 75306-007-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020
3	NDC: 75306-007-02	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020
4	NDC: 75306-007-03	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020
5	NDC: 75306-007-04	120 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020
6	NDC: 75306-007-05	150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020
7	NDC: 75306-007-06	160 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020
8	NDC: 75306-007-07	200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020
9	NDC: 75306-007-08	250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020
10	NDC: 75306-007-09	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020
11	NDC: 75306-007-10	1000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020
12	NDC: 75306-007-11	3785 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020
13	NDC: 75306-007-12	18927 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020
14	NDC: 75306-007-13	5000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020
15	NDC: 75306-007-14	10000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020
16	NDC: 75306-007-15	15000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020
17	NDC: 75306-007-16	20000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2020

Labeler - D-Time Limited Liability Company (081728006)

Establishment
Name	Address	ID/FEI	Business Operations
D-Time Limited Liability Company		081728006	manufacture(75306-007)