Hand Sanitizer130

Hand Sanitizer130

Drug Labeling and Warnings

Drug Details

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ETHYL ALCOHOL- ethyl alcohol gel 
Wal-Mart Stores, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Hand Sanitizer
130

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.
• avoid contact with broken skin
• do not inhale or 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, glycerin, propylene glycol, fragrance, acrylates/C10-30 alkyl acrylate crosspolymer, triethanolamine, blue 1, red 40, yellow 5

Product of China

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

Distributed by: Walmart Inc., Bentonville, AR 72716

130.000/130AA

Principal display panel

49035-418-10

equate

Hand Sanitizer

Sandalwood & Sea

Kills 99.99% of germs*

Contains moisturizers

1 FL OZ (29.5 mL)

ETHYL ALCOHOL 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49035-418
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	620 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
TRIETHANOLAMINE LACTATE (UNII: 064C51N81O)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49035-418-10	29.5 mL in 1 PACKAGE; Type 0: Not a Combination Product	01/03/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/03/2020

Labeler - Wal-Mart Stores, Inc. (051957769)

Registrant - Vi-Jon, Inc. (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, Inc.		088520668	manufacture(49035-418)

Revised: 1/2020

Document Id: 10279341-0f43-468f-8710-f60ad55e7a57

34390-5

Set id: f7d9bb83-0b80-458b-9554-8adbe51473e4

Version: 5

Effective Time: 20200103

 

Wal-Mart Stores, Inc.