Hand Sanitizer by NINGBO MEITELI COSMETICS CO., LTD HAND SANITIZER gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by NINGBO MEITELI COSMETICS CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

ETHYL ALCOHOL 75%

Purpose

Antiseptic

Use

Use Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

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

Do not use

Do not use
●on open skin wounds.
●on children less than 2 years of age.

WHEN USING

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

STOP USE

Stop use and ask a doctor if imitation or rash occurs. These may be signs of a serious condition.

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

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

1.Store between 15-30"C(59-86*F)
2.Avoid freezing and excessive heat above 40°C(104°F)

Inactive ingredients

Water (Aqua),Carbomer, Aminomethyl propanol Butylene glycol, Aloe barbadensis leaf extract

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75541-015
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
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75541-015-01	54 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/18/2024
2	NDC: 75541-015-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/18/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	09/18/2024

Labeler - NINGBO MEITELI COSMETICS CO., LTD (546624772)

Establishment
Name	Address	ID/FEI	Business Operations
NINGBO MEITELI COSMETICS CO., LTD		546624772	manufacture(75541-015)