Hand Sanitizer by Rite Aid / Vi-Jon Drug Facts 

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Rite Aid, Vi-Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER- ethyl alcohol gel 
Rite Aid

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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Drug Facts 

Active ingredients

Ethyl Alcohol 65%

Purpose

Antiseptic

Use

Use

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

Warnings

For external use only-hands

Flammable

 Keep away from heat and flame

when using

When using this product

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

Stop use

and ask a doctor if skin irritation develops

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 dr 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

benzopheone-4, butyrospermum parkii (shea butter), carbomer, cellulose, fragrance, glycerin, hydroxypropyl methylcellulose, iron oxides, isopropyl myristate, mannitol, propylene glycol, tocopheryl acetate, water

Claims

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

Made in USA with US and foreign components

Adverse Reactions

Distributedm by Rite Aid

30 Hunter Lane, Camp Hill, PA17011

principal display panel

RITE

AID

RENEWAL

instant

HAND SANITIZER

WITH SHEA BUTTER

Kills 99.99% of Germs

Leaving Hands Feeling

Soft And Refreshed

8 FL OZ (236 mL)

HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-0440
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	585 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SULISOBENZONE (UNII: 1W6L629B4K)
SHEA BUTTER (UNII: K49155WL9Y)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
GLYCERIN (UNII: PDC6A3C0OX)
HYPROMELLOSES (UNII: 3NXW29V3WO)
FERRIC OXIDE RED (UNII: 1K09F3G675)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
MANNITOL (UNII: 3OWL53L36A)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-0440-8	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	07/12/2010	04/13/2020
2	NDC: 11822-0440-2	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/12/2010	04/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/12/2010	04/13/2020

Labeler - Rite Aid (014578892)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		088520668	manufacture(11822-0440)

Revised: 4/2020

Document Id: 6ed6747e-f2bf-4861-ae2a-cec28acf5de5

34390-5

Set id: f0b0c4f2-ad19-4691-958b-7480b8cd94df

Version: 4

Effective Time: 20200413

 

Rite Aid