SKINTILLATE HAND SANITIZER- alcohol liquid

Skintillate Hand Sanitizer by

Drug Labeling and Warnings

Skintillate 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

Alcohol 80% v/v.

Purpose

Antiseptic skin cleanser

Use

For personal hand hygiene to help prevent the spread of bacteria

Warning

For external use only
When using this product avoid contact with eyes.
Flammable. Keep away from heat and flame.

Ask doctor

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.

Inactive ingredients

Water, Isopropyl alcohol, Glycerin, Hyaluronic Acid, Bergamot leaf oil, Lavender Flower, Hydrogen Peroxide, Centella Asiatica Extract, Sodium pyruvate 

Other information

Store at 68 to 70 F (20 to 25 C). May discolor certain fabrics on surfaces

Questions?

1-844-800-6858

package

INGREDIENTS AND APPEARANCE

SKINTILLATE HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75306-005
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)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
HYALURONIC ACID (UNII: S270N0TRQY)
BERGAMOT OIL (UNII: 39W1PKE3JI)
LAVENDER OIL (UNII: ZBP1YXW0H8)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
SODIUM PYRUVATE (UNII: POD38AIF08)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75306-005-01	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020
2	NDC: 75306-005-02	50 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020
3	NDC: 75306-005-03	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020
4	NDC: 75306-005-04	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020
5	NDC: 75306-005-05	120 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020
6	NDC: 75306-005-06	150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020
7	NDC: 75306-005-07	160 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020
8	NDC: 75306-005-08	200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020
9	NDC: 75306-005-09	250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020
10	NDC: 75306-005-10	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020
11	NDC: 75306-005-11	1000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020
12	NDC: 75306-005-12	3785 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020
13	NDC: 75306-005-13	18927 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020
14	NDC: 75306-005-14	5000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020
15	NDC: 75306-005-15	10000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020
16	NDC: 75306-005-16	15000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020
17	NDC: 75306-005-17	20000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/21/2020

Labeler - D-Time Limited Liability Company (081728006)

Establishment
Name	Address	ID/FEI	Business Operations
D-Time Limited Liability Company		081728006	manufacture(75306-005)