DR.BETTER HOMES HAND CLEAN- alcohol gel

Dr.Better Homes Hand Clean by

Drug Labeling and Warnings

Dr.Better Homes Hand Clean by is a Otc medication manufactured, distributed, or labeled by UI COSMETICS CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol

INACTIVE INGREDIENT

Water, Glycerin, Carbomer, Triethanolamine, Fragrance

PURPOSE

Antiseptic

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

For the external use only

WARNINGS

Do not use on the following body parts.
Around the eyes and ears, in the oral cavity, a wide range of body parts and damaged skin (may have irritating effects)
If the following symptoms appear, stop using them immediately and consult a doctor or pharmacist.

Symptoms of skin irritation

Other precautions

For external use only
Be careful not to get into your eyes, and if so, rinse well with clean water and consult a doctor or pharmacist.
Be careful not to inhale vapor when using it extensively or for a long time. (If you drink ethanol vapor in large quantities or repeatedly, irritation to the mucous membrane, headache, etc. may occur).
When repeated use on the same site, be careful as the skin may become rough due to degreasing.
When used in sealed bandages, cast bandages, packs, etc., irritation symptoms may appear.
Do not use for any other purpose.

DOSAGE & ADMINISTRATION

Put a suitable amount on your hand and rub it well to dry

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR.BETTER HOMES HAND CLEAN 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75615-0010
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
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75615-0010-1	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	part333A	04/01/2020

Labeler - UI Cosmetics Co., Ltd. (688362189)

Establishment
Name	Address	ID/FEI	Business Operations
UI Cosmetics Co., Ltd.		688362189	label(75615-0010)

Establishment
Name	Address	ID/FEI	Business Operations
Sangji Enterprise Co.,LTD Cheongwon Oriental Medical Cosmetic Branch		695625894	manufacture(75615-0010)