Alcohol by Amazon.com Services LLC / Vi Jon, LLC / Vi-Jon, LLC ALCOHOL liquid

Alcohol by

Drug Labeling and Warnings

Alcohol by is a Otc medication manufactured, distributed, or labeled by Amazon.com Services LLC, Vi Jon, LLC, 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 eyues, flush thoroughly with water
• avoid 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

Disclaimer

*Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

 DSP-TN-21091   DSP-MO-20087  DSP-MO-28  SDS-MO-20068

Adverse Reaction

DISTRIBUTED BY: Amazon.com Services LLC

Seattle, WA 98109   1-877-485-0385

©2023 Amazon.com, Inc. or its affiliates. All rights reserves. Amazon Basic Care and all related logos are trademarks of Amazon.com, Inc or its affiliates.

Principal display panel

amazon

basic care

With Aloe & Vitamin E

Moisturizing Hand Sanitizer

Kills 99.99% of Germs*

34 FL OZ (1.06 QT) 1L

INGREDIENTS AND APPEARANCE

ALCOHOL 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72288-826
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
WATER (UNII: 059QF0KO0R)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ALOE (UNII: V5VD430YW9)
TOCOPHEROL (UNII: R0ZB2556P8)
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: 72288-826-48	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/04/2021
2	NDC: 72288-826-32	354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/04/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/04/2021

Labeler - Amazon.com Services LLC (128990418)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(72288-826)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(72288-826)