DR. DADDYS HAND SANITIZER- alcohol gel

Dr. Daddys Hand Sanitizer by

Drug Labeling and Warnings

Dr. Daddys Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by TB Healthcare Co., Ltd., K.Boeun Pharmaceutical Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol

INACTIVE INGREDIENT

Water, Glycerin, Triethanolamine, Carbomer, Green Tea Extract, Aloe Extract, Sage Extract, Matricaria(Chamomilla) Extract

PURPOSE

Antimicrobial

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

■ Store between 1-30C

■ Avoid freezing and excessive heat above 40C

WARNINGS

For external use only. Flammable, Keep away from fire or flames.
Do not use

■ in children less than 2 months of age

■ on open skin wounds
when using this product keep out of eyes, ears, and mouth.
Stop use and ask a doctor if irritation or rash occurs. these may be signs of a serious condition.
Keep out of reach of children. if swallowed, get medical help or contact a poison control center right away.

DOSAGE & ADMINISTRATION

■ Place enough product on hands to cover all surfaces. Rub hands together until dry.

■ Supervise children under 6 years of age when using this product to avoid swallowing.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR. DADDYS HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76884-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	42 mL  in 60 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE (UNII: V5VD430YW9)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
CHAMOMILE (UNII: FGL3685T2X)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76884-0002-1	60 mL in 1 TUBE; 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 - TB Healthcare Co., Ltd. (695035143)

Registrant - TB Healthcare Co., Ltd. (695035143)

Establishment
Name	Address	ID/FEI	Business Operations
TB Healthcare Co., Ltd.		695035143	label(76884-0002)

Establishment
Name	Address	ID/FEI	Business Operations
K.Boeun Pharmaceutical Co.,Ltd.		695674074	manufacture(76884-0002)