TNS MEDIPLUS HAND SANITIZER- ethyl alcohol gel

TNS MEDIPLUS HAND SANITIZER by

Drug Labeling and Warnings

TNS MEDIPLUS HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Nature Intro Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl alcohol 72% v/v

INACTIVE INGREDIENTS

Water, carbomer, aloe extract, green tea extract, sodium hyaluronate, aminomethyl propanol, glycerin, orange oil, polysorbate 20, potassium hydroxide, tocopheryl acetate

PURPOSE

ANTISEPTIC

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.

Use(s)

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

For use when soap and water are not available.

Directions

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.

Other Information

Store between 15-30℃ (59-86℉)
Avoid freezing and excessive heat above 40℃ (104℉)

Package Label: TNS MEDIPLUS HAND SANITIZER 100mL

Package Label: TNS MEDIPLUS HAND SANITIZER 500mL

Package Label: TNS MEDIPLUS HAND SANITIZER 1000mL

INGREDIENTS AND APPEARANCE

TNS MEDIPLUS HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78222-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	72 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ALOE (UNII: V5VD430YW9)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
Glycerin (UNII: PDC6A3C0OX)
ORANGE OIL (UNII: AKN3KSD11B)
polysorbate 20 (UNII: 7T1F30V5YH)
potassium hydroxide (UNII: WZH3C48M4T)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78222-010-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020
2	NDC: 78222-010-02	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/01/2020
3	NDC: 78222-010-03	1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/01/2020

Labeler - Nature Intro Co., Ltd. (688282814)

Registrant - Nature Intro Co., Ltd. (688282814)

Establishment
Name	Address	ID/FEI	Business Operations
Nature Intro Co., Ltd.		688282814	manufacture(78222-010)