DR. SAFE CLEAN- alcohol gel

Dr. Safe Clean by

Drug Labeling and Warnings

Dr. Safe Clean 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 70%

INACTIVE INGREDIENT

Inactive ingredients:

Water, Glycerlin, Triethanolamine, Carbomer, Gardenia Florida Fruit Extract

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:
Put enough product in your palm and rub hands together until dry.
For children under 6 years, use only under adult supervision.

Other information

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

PACKAGE LABEL - Dr. Safe Clean Gel 70mL

PACKAGE LABEL - Dr. Safe Clean Gel 500mL

INGREDIENTS AND APPEARANCE

DR. SAFE CLEAN 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76369-8090
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76369-8090-1	70 mL in 1 CONTAINER; Type 0: Not a Combination Product	04/01/2020
2	NDC: 76369-8090-2	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/01/2020

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

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(76369-8090)