SKINTILLATE HAND SANITIZER- alcohol, isopropyl alcohol solution

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 Ingredients

Alcohol (80%)
Ethyl Alcohol (75%), Isopropyl Alcohol (5%)

​Purpose

Antiseptic skin cleanser

Use

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

Warnings

For external use only.

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.

Flammable. Keep away from heat and flame.

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

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

Other information
Store at 680 to 700 F (200 to 250C). May discolor certain fabrics or surfaces.
Questions? 1-844-800-6858

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

SKINTILLATE HAND SANITIZER 
alcohol, isopropyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75306-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	5 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
GLYCERIN (UNII: PDC6A3C0OX)
HYALURONIC ACID (UNII: S270N0TRQY)
BERGAMOT OIL (UNII: 39W1PKE3JI)
LAVENDER OIL (UNII: ZBP1YXW0H8)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
SODIUM PYRUVATE (UNII: POD38AIF08)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75306-003-01	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2020
2	NDC: 75306-003-02	50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2020
3	NDC: 75306-003-03	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2020
4	NDC: 75306-003-04	100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2020
5	NDC: 75306-003-05	120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2020
6	NDC: 75306-003-06	160 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2020
7	NDC: 75306-003-07	200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2020
8	NDC: 75306-003-08	250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2020

Labeler - D-Time Limited Liability Company (081728006)

Establishment
Name	Address	ID/FEI	Business Operations
D-Time Limited Liability Company		081728006	manufacture(75306-003)