Label: LILKOI HAND SANITIZER- ethyl alcohol spray
-
Contains inactivated NDC Code(s)
NDC Code(s): 75306-007-01, 75306-007-02, 75306-007-03, 75306-007-04, view more75306-007-05, 75306-007-06, 75306-007-07, 75306-007-08, 75306-007-09, 75306-007-10, 75306-007-11, 75306-007-12, 75306-007-13, 75306-007-14, 75306-007-15, 75306-007-16, 75306-007-17 - Packager: D-Time Limited Liability Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated November 2, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- KEEP OUT OF REACH OF CHILDREN
-
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
- Lilkoi hand sanitizer
-
INGREDIENTS AND APPEARANCE
LILKOI HAND SANITIZER
ethyl alcohol sprayProduct 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)
