PURELOGIC HAND SANITIZER GREEN TEA ALOE- alcohol solution

PureLogic Hand Sanitizer Green Tea Aloe by

Drug Labeling and Warnings

PureLogic Hand Sanitizer Green Tea Aloe by is a Otc medication manufactured, distributed, or labeled by Argento sc by sicura inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 75% v/v

PURPOSE

Purpose: 

Antimicrobial

Use

Decrease bacteria on skin that could cause disease

Recommended for repeated use

Warnings

For external use only. Flammable, keep way from flame or fire

When using this product

When using this product, keep out of eyes. In case of contact with eyes, flush thoroughly with water

Do not ingest or inhale

Avoid contact with broken skin

Stop use and ask a doctor

if irrigation and redness develop or if condition persists for more than 72 hours

Keep out of reach of children

if swallowed,get medical help or contact a Poison Control Center immediately

Directions

• Spread product on hands thoroughly and allow to dry, do not wipe off
• For children under 6, use under adult supervision
• Not recommended for use with infants

Other information

Do not store above 105F (40.6C)

May discolor some fabrics

Harmful to plastics and wood finishes

Inactive ingredients

Purified water, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E), Fragrance, Blue 1 (CI42090), Yellow 5 (CI19140)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURELOGIC HAND SANITIZER GREEN TEA ALOE 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77731-040
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
CARBOMER 940 (UNII: 4Q93RCW27E)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77731-040-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/30/2020

Labeler - Argento sc by sicura inc. (168718778)