USANA Hand Sanitizer by USANA Health Sciences, Inc. / Dynamic Blending Specialists, Inc. USANA Hand Sanitizer

USANA Hand Sanitizer by

Drug Labeling and Warnings

USANA Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by USANA Health Sciences, Inc., Dynamic Blending Specialists, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

USANA HAND SANITIZER- alcohol liquid 
USANA Health Sciences, 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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USANA Hand Sanitizer

Drug Facts

Active Ingredient(s)

Alcohol 70% v/v

Purpose

Antiseptic

Uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use

• On open skin wounds.
• In children less than 2 months of age

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. 

Stop use and ask a doctor if irritation or rash occurs.

These may be signs of a serious condition.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing

Other information:

• Store between 15-30ºC. (59-86ºF)
• Avoid freezing and excessive heat above 40ºC. (104ºF)

Inactive ingredients:

Water, Ammonium Acryloyldimethyltaurate/ VP Copolymer, Hydrogen Peroxide, Aloe Barbadensis Leaf Juice, Mixed Tocopherols, Polysorbate 20, Cymbopogon Flexuosus (Lemongrass) Herb Oil, Citrus Sinensis (Sweet Orange) Peel Oil Expressed.

Questions or comments?

Call toll free 1-800-950-9595.

Package Labeling:

USANA HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51861-071
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
AMMONIUM ACRYLOYLDIMETHYLTAURATE (UNII: KBC00G95HI)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TOCOPHEROL (UNII: R0ZB2556P8)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
CYMBOPOGON CITRATUS LEAF (UNII: 06JMS448M5)
ORANGE PEEL (UNII: TI9T76XD44)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51861-071-01	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/07/2020	12/28/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	09/07/2020	12/28/2021

Labeler - USANA Health Sciences, Inc. (804413250)

Establishment
Name	Address	ID/FEI	Business Operations
Dynamic Blending Specialists, Inc.		085704438	manufacture(51861-071)

Revised: 2/2023

Document Id: f3bd1642-1f1b-f812-e053-2a95a90af945

34390-5

Set id: 8c51427b-d1f1-4c6e-8423-89e36d161c74

Version: 3

Effective Time: 20230202