AL-SHIELDS- ethyl alcohol gel

al-SHIELDS by

Drug Labeling and Warnings

al-SHIELDS by is a Otc medication manufactured, distributed, or labeled by Yozzi Co.,ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Ethyl Alcohol 75% v/v

Purpose

Antimicrobial

Uses

Hand Sanitizer to help reduce bacteria on the skin

Warnings

Flammable. Keep away from fire or flame.

For external use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts

Keep out of reach of children.

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

Directions

• Wet hands thoroughly with product and briskly rub hands together until dry
• Children under the age of 6 should be supervised by an adult when using this product

Other Information

• Store below 105°F (40°C)
• May discolor certain fabrics

Inactive ingredients

Water (Aqua), Glycerin, Propylene Glycol, Carbomer, Aminomethyl propanol Aloe Barbadensis (Aloe Vera) Gel, Tocopheryl Acetate (Vitamin E)

SPL UNCLASSIFIED SECTION

KILLS 99.99% OF GERMS

75% ALCOHOL

WITH MOISTURIZERS

ORIGINAL SCENT

SHOP WITH US AT

WWW.AL-SHIELDS.COM

QUESTIONS? CONTANT US AT

CONTACTUS@AL-SHIELDS.COM

DISTRIBUTED BY:

GMA GROUP

3 EMPIRE BOULEVARD

SOUTH HACKENSACK,

NY07676

MADE IN CHINA

Packaging

INGREDIENTS AND APPEARANCE

AL-SHIELDS 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72285-011
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
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72285-011-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/16/2020
2	NDC: 72285-011-05	2 in 1 BLISTER PACK	07/16/2020
2	NDC: 72285-011-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 72285-011-06	3 in 1 BLISTER PACK	07/16/2020
3	NDC: 72285-011-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC: 72285-011-03	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/16/2020
5	NDC: 72285-011-02	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/16/2020
6	NDC: 72285-011-04	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/16/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/16/2020

Labeler - Yozzi Co.,ltd (560426393)

Establishment
Name	Address	ID/FEI	Business Operations
Yozzi Co.,ltd		560426393	manufacture(72285-011)