ADVANCED HAND SANITIZER liquid

Advanced Hand Sanitizer by

Drug Labeling and Warnings

Advanced Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Ningbo Meiteli Cosmetic Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 70%

Purpose

Antimicrobial

Use

Hand Sanitizer to help reduce bacteria on the skin.

Warning

Flammable. Keep away from heat or flame

For external use only.

Do not use near eyes

In case of contact rinse eyes thoroughly with water.

Stop use

Stop use and see a doctor if imtation or rash appears and lasts

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 enough sanitizer in your palm to cover both hands,Rub hands together brishly until dry,Children under six should be supervised

Other

• Store below 110F(43C)
• May discolor some fabrics or surfaces

Inactive ingredients

Alcohol Denat,Water(aqua),Glycerin,Carbomer,Aminomethylpropanol,Aloe Barbadensis Leaf Juice,Tocopherol

WHEN USING

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

ADVANCED HAND SANITIZER 
advanced hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75541-005
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
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER 934 (UNII: Z135WT9208)
WATER (UNII: 059QF0KO0R)
ALOE (UNII: V5VD430YW9)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75541-005-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
2	NDC: 75541-005-02	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
3	NDC: 75541-005-03	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020
4	NDC: 75541-005-04	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/22/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/22/2020

Labeler - Ningbo Meiteli Cosmetic Co., Ltd. (546624772)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Meiteli Cosmetic Co., Ltd.		546624772	manufacture(75541-005)