SANIPRO HAND SANITIZER 70 500ML- ethyle alcohol gel

SANIPRO Hand Sanitizer 70 500ml by

Drug Labeling and Warnings

SANIPRO Hand Sanitizer 70 500ml by is a Otc medication manufactured, distributed, or labeled by E.CIS COSMETIC.Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

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

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

Stop use and ask a doctor

Stop use and ask a doctor if irritation 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

• 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 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Water, Glycerin, Carbomer, Aminomethyl Propanol, Mentha Arvensis Leaf Oil, Aloe Barbadensis Leaf Extract, Panthenol, Sodium Hyaluronate, Salvia Officinalis (Sage) Leaf Extract

Package Label - Principal Display Panel

SANIPRO
HAND SANITIZER
WITH ALOE MOISTURIZER
SAFELY
CLEANS & CONDITIONS
PF SF
PARABEN & SULFATE FREE
16.9 FL.OZ. (500ML)

INGREDIENTS AND APPEARANCE

SANIPRO HAND SANITIZER 70 500ML 
ethyle alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73862-215
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 940 (UNII: 4Q93RCW27E)
WATER (UNII: 059QF0KO0R)
MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
PANTHENOL (UNII: WV9CM0O67Z)
SAGE (UNII: 065C5D077J)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73862-215-11	24 in 1 CASE	03/30/2020
1	NDC: 73862-215-10	500 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - E.CIS COSMETIC.Co.,Ltd (689846270)

Establishment
Name	Address	ID/FEI	Business Operations
E.CIS COSMETIC.Co.,Ltd		689846270	manufacture(73862-215)