FIRST SAFETY INSTANT HAND SANITIZER- alcohol gel

First Safety Instant Hand Sanitizer by

Drug Labeling and Warnings

First Safety Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Ningbo Mannike Biological Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                                  Purpose

Ethyl Alcohol                70%      ...        Antiseptic

PURPOSE

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

KEEP OUT OF REACH OF CHILDREN

If swallowed, get meical help or contact Poison Control Center right away.

INDICATIONS & USAGE

keep out of eyes,ears, and 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 a serious condition.

WARNINGS

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

Do not use:

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

DOSAGE & ADMINISTRATION

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

INACTIVE INGREDIENT

Glycerin, Aloe， water, Barbadensis gel, Carbomer

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FIRST SAFETY INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75780-008
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)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER 934 (UNII: Z135WT9208)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75780-008-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
2	NDC: 75780-008-02	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
3	NDC: 75780-008-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/15/2020

Labeler - Ningbo Mannike Biological Technology Co., Ltd. (413126185)

Establishment
Name	Address	ID/FEI	Business Operations
Ningbo Mannike Biological Technology Co., Ltd.		413126185	manufacture(75780-008)