DR CLEAN PERFECT GEL- alcohol spray

Dr Clean PERFECT Gel by

Drug Labeling and Warnings

Dr Clean PERFECT Gel by is a Otc medication manufactured, distributed, or labeled by Handock Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient: ALCOHOL 68% (v/v)

INACTIVE INGREDIENT

Inactive ingredients:

Water, Propylene Glycol, Glycerlin, Triethanolamine, Carbomer

PURPOSE

Purpose: Antiseptic

WARNINGS

Warnings:

For external use only. Flammable.
Keep away from flame and fire.

When using this product
Keep out of eyes.
In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if
irritation or redness develops and lasts.

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.

Uses

Uses:

Hand sanitizer to help reduce bacteria on the skin.
Recommended for repeated use.

Directions

Directions:
Spray directly on hands and rub in thoroughly.
For children under 6 years, use only under adult supervision.
Not recommended for infants

Other information

Other information:
Store below 110°F (43°C)
may discolor some fabrics or surfaces

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR CLEAN PERFECT GEL 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76369-8080
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	68 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Propylene Glycol (UNII: 6DC9Q167V3)
Glycerin (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76369-8080-1	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/01/2020

Labeler - Handock Cosmetics Co., Ltd. (688037204)

Registrant - Handock Cosmetics Co., Ltd. (688037204)

Establishment
Name	Address	ID/FEI	Business Operations
Handock Cosmetics Co., Ltd.		688037204	manufacture(76369-8080)