LILKOI HAND SANITIZER- ethyl alcohol spray 
D-Time Limited Liability Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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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.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

image description

LILKOI HAND SANITIZER 
ethyl alcohol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75306-007
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALMOND OIL (UNII: 66YXD4DKO9)  
LAVENDER OIL (UNII: ZBP1YXW0H8)  
HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
SODIUM PYRUVATE (UNII: POD38AIF08)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75306-007-1730 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/2020
2NDC:75306-007-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/2020
3NDC:75306-007-0260 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
4NDC:75306-007-03100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
5NDC:75306-007-04120 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
6NDC:75306-007-05150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
7NDC:75306-007-06160 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
8NDC:75306-007-07200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
9NDC:75306-007-08250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
10NDC:75306-007-09500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
11NDC:75306-007-101000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
12NDC:75306-007-113785 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
13NDC:75306-007-1218927 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
14NDC:75306-007-135000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
15NDC:75306-007-1410000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
16NDC:75306-007-1515000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
17NDC:75306-007-1620000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/01/2020
Labeler - D-Time Limited Liability Company (081728006)
Establishment
NameAddressID/FEIBusiness Operations
D-Time Limited Liability Company081728006manufacture(75306-007)

Revised: 11/2021
Document Id: cfd13ff1-88fb-39c7-e053-2a95a90a0986
Set id: 40ae1f0f-e65d-4f51-96d4-dee2d89dda9d
Version: 2
Effective Time: 20211102
 
D-Time Limited Liability Company