OLIKA ULTRA HYDRATING HAND SANITIZER FRAGRANCE FREE- alcohol gel

Olika Ultra Hydrating Hand Sanitizer Fragrance Free by

Drug Labeling and Warnings

Olika Ultra Hydrating Hand Sanitizer Fragrance Free by is a Otc medication manufactured, distributed, or labeled by Amyris, Inc, Taizhou Jingshang Cosmetics Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 65% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

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

• in children less than 2 months of age
• on open skin wounds

WHEN USING

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.

STOP USE

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

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 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Aqua
Glycerin
Aloe Barbadensis Leaf Extract
Sodium Hyaluronate

Package Label - Principal Display Panel

Label 30 ml NDC: 73517-111-01

Label 20 ml NDC: 73517-111-02

Label 90 ml NDC: 73517-111-03

INGREDIENTS AND APPEARANCE

OLIKA ULTRA HYDRATING HAND SANITIZER FRAGRANCE FREE 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73517-111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73517-111-02	30 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	09/01/2021
2	NDC: 73517-111-03	20 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	09/01/2021
3	NDC: 73517-111-01	90 mL in 1 POUCH; Type 0: Not a Combination Product	09/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/30/2020

Labeler - Amyris, Inc (185930182)

Establishment
Name	Address	ID/FEI	Business Operations
Taizhou Jingshang Cosmetics Technology Co., Ltd.		550819554	manufacture(73517-111)