ALLY HAND SANITIZER WIPES- alcohol cloth

Ally Hand Sanitizer Wipes by

Drug Labeling and Warnings

Ally Hand Sanitizer Wipes by is a Otc medication manufactured, distributed, or labeled by Guy & O'Neill, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Use

to decrease bacteria on the skin

Warnings

For external use only: hands

Flammable. Keep away from heat and flame.

When using this product

• keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• avoid contact with broken skin
• do not inhale or ingest

Stop use and ask a doctor if

• irritation or redness develops
• condition persists for more than 72 hours

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• wet hands thoroughly with the product and allow to dry without wiping
• not recommended for infants

Other Information

• do not store above 105°F
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive ingredients

Aloe barbadensis leaf juice, glycerin, isopropanol, propanediol, tocopheryl acetate, water

Questions?

1-844-342-6691

PRINCIPAL DISPLAY PANEL - 20 Wipe Pouch

ally®

HAND
SANITIZING WIPES

Kills 99.99% of
Germs Instantly*

Fast and Effective
70% Ethyl Alcohol

Enriched with Moisturizers
Aloe and Vitamin E

037198R

To Open Peel Back
Resealable Label

20 Wipes
5.5in x 8.4in (13.9cm x 21.3cm)

DO NOT FLUSH

INGREDIENTS AND APPEARANCE

ALLY HAND SANITIZER WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50862-1310
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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	29 mL
ISOPROPYL ALCOHOL (UNII: ND2M416302)	1 mL
GLYCERIN (UNII: PDC6A3C0OX)	1 mL
PROPANEDIOL (UNII: 5965N8W85T)	0.5 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.1 mL
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)	0.001 mL

Product Characteristics
Color		Score	no score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50862-1310-4	20 in 1 POUCH; Type 0: Not a Combination Product	04/05/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH DRUG	M003	04/05/2022

Labeler - Guy & O'Neill, Inc. (037838844)

Registrant - Guy & O'Neill, Inc. (037838844)

Establishment
Name	Address	ID/FEI	Business Operations
Guy & O'Neill, Inc.		037838844	MANUFACTURE(50862-1310) , LABEL(50862-1310)