Alcohol by United Natural Foods, Inc. dba UNFI / Vi Jon, LLC ALCOHOL liquid

Alcohol by

Drug Labeling and Warnings

Alcohol by is a Otc medication manufactured, distributed, or labeled by United Natural Foods, Inc. dba UNFI, Vi Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

  Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

• to decrease bacteria on the skin that could cause disease
• recommended for repeated use

Warnings

For external use only: hands

Flammable, keep away from fire or flame

When using this product

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

Stop use and ask a doctor if

• irritation and redness develop
• 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 product and allow to dry without wiping
• for children under 6, use only under adult supervision
• not recommended for infants

Other information

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

Inactive ingredients

water, carbomer, fragrance, glycerin, isopropyl myristate, Aloe barbadensis leaf juice, tocopheryl acetate, blue 1, yellow 5

Adverse reaction

Like it or let us make it right.

That's our quality promise.

855-423-2630

DISTRIBUTED BY UNFI

PROVIDENCE, RI 02968 USA

Principal display panel

EQUALINE

MOISTURIZING

Hand Sanitizer

with Aloe and Vitamine E

2 FL OZ (59 mL)

INGREDIENTS AND APPEARANCE

ALCOHOL 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41163-826
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
GLYCERIN (UNII: PDC6A3C0OX)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE (UNII: V5VD430YW9)
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: 41163-826-34	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/13/2022
2	NDC: 41163-826-16	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/13/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/13/2022

Labeler - United Natural Foods, Inc. dba UNFI (943556183)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(41163-826)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(41163-826)