MASK ON EVERY FACE VITAMIN E ALOE HAND SANITIZER- alcohol gel

Mask on Every Face Vitamin E Aloe Hand Sanitizer by

Drug Labeling and Warnings

Mask on Every Face Vitamin E Aloe Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Taizhou Yadai Daily-Use Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 75% v/v

Purpose

Antiseptic

Use

Hand sanitizer to help decrease bacteria that potentially can cause disease

For use when soap and water are not available

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use 

• In children less than 2 months of age
• On open skin wounds

When using this product, keep out of eyes, ears or mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs, these may be signs of serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get immediate medical help or contact a Poison Control Center right away.

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

Inactive ingredients

Water, Aminomethylpropanol, Carbomer 940, Aloe Vera Leaf, Alpha Tocopherol Acetate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MASK ON EVERY FACE VITAMIN E ALOE HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52989-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER 940 (UNII: 4Q93RCW27E)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52989-005-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/06/2020
2	NDC: 52989-005-02	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/06/2020
3	NDC: 52989-005-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/06/2020
4	NDC: 52989-005-04	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/06/2020
5	NDC: 52989-005-05	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/06/2020
6	NDC: 52989-005-06	53 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/06/2020
7	NDC: 52989-005-07	75 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/06/2020
8	NDC: 52989-005-08	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/06/2020
9	NDC: 52989-005-09	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/06/2020
10	NDC: 52989-005-10	350 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/06/2020

Labeler - Taizhou Yadai Daily-Use Co., Ltd. (529899639)

Establishment
Name	Address	ID/FEI	Business Operations
Taizhou Yadai Daily-Use Co., Ltd.		529899639	manufacture(52989-005)