DR PLUS MEDM HAND SANITIZER- alcohol gel

Dr Plus MEDM Hand Sanitizer by

Drug Labeling and Warnings

Dr Plus MEDM Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Dermal Korea Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ETHYL ALCOHOL 70% v/v

INACTIVE INGREDIENT

Purified Water USP, Glycerin, Carbomer, Triethanolamine, Tocopheryl Acetate, Sodium Hyaluronate, Aloe Barbadensis Leaf Extract, Camellia Sinensis Leaf Extract, Morus Alba Bark Extract, Disodium EDTA, 1,2-Hexanediol, Fragrance

PURPOSE

ANTISEPTIC

WARNINGS

Warnings:

For external use only. Flammable. Keep away from heat or flame
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Do not use
in children less than 2 months of age
on open skin wounds
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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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.

Uses

Uses

For hand washing to help reduce bacteria on the skin.
Recommended for repeated use

Directions

Directions

Place sufficient amount on both hands and spread evenly before drying.
Do not use other than directed

Other Information

Store between 15-30C (59-86F)

Avoid freezing and excessive heat above 40C (104F)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR PLUS MEDM HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71882-103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	Alcohol	350 mL  in 500 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
MORUS ALBA BARK (UNII: 7O71A48NDP)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
1,2-Hexanediol (UNII: TR046Y3K1G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71882-103-01	500 mL in 1 BOTTLE, PUMP; 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	part333E	05/01/2020

Labeler - Dermal Korea Co., Ltd (688990247)

Registrant - Dermal Korea Co., Ltd (688990247)

Establishment
Name	Address	ID/FEI	Business Operations
Dermal Korea Co., Ltd		688990247	manufacture(71882-103)