M MARVEL SANI CARE INSTANT HAND SANITIZER- alcohol gel

M MARVEL SANI CARE Instant Hand Sanitizer by

Drug Labeling and Warnings

M MARVEL SANI CARE Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by GUANGZHOU TECHIN DEVELOPMENT CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Use

For daily hand sanitizing, to reduce bateria on hands

Warnings

For external use only

Flammable. Keep away from fires and high temperature

WHEN USING

Do not use on open skin wounds

Avoid eyes. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

Stop use if irritation or rash occurs, if condition persists, contact a healthcare proactitioner

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.

Directions

• Put proper amount onto palms and rub hands briskly until dry.
• No washing or rinsing required. Air dries quickly

Other information

Keep in closed container in a cool dry place of ambient temperature between 5-30C (59-86F)

Batch and MFG date printed on bottle

Validity: 24 mounths from MFG date

Made in China

Inactive ingredients

Water, Aminomethyl propanol, aloe vera extract, glycerin, carbomer, D-Panthenol, vitamin E

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

M MARVEL SANI CARE INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80107-001
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER 940 (UNII: 4Q93RCW27E)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PANTHENOL (UNII: WV9CM0O67Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80107-001-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/26/2020
2	NDC: 80107-001-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/26/2020
3	NDC: 80107-001-03	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/26/2020
4	NDC: 80107-001-04	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/26/2020
5	NDC: 80107-001-05	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/26/2020
6	NDC: 80107-001-06	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/26/2020

Labeler - GUANGZHOU TECHIN DEVELOPMENT CO., LTD (527219392)

Establishment
Name	Address	ID/FEI	Business Operations
GUANGZHOU TECHIN DEVELOPMENT CO., LTD		527219392	manufacture(80107-001)