DR CLEAN PERFECT CARE GEL- alcohol spray
Handock Cosmetics Co., Ltd.

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

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

Image of bottle

DR CLEAN PERFECT CARE GEL
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:76369-8070
Route of Administration	TOPICAL

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

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76369-8070-1	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/01/2020	04/02/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	03/01/2020	04/02/2020

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

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

Name	Address	ID/FEI	Business Operations
Establishment
Handock Cosmetics Co., Ltd.		688037204	manufacture(76369-8070)

Revised: 4/2020

Document Id: 9b1e5a8f-ee4e-42a2-a875-e4e8f28394a5

Set id: 3c0fc209-9aca-4280-a715-dfb093137c62

Version: 3

Effective Time: 20200403

Handock Cosmetics Co., Ltd.