OLIKA ULTRA HYDRATING HAND SANITIZER FRAGRANCE FREE- alcohol gel 
Amyris, 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.

----------

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

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 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

Other information

Inactive ingredients

aloe vera (aloe barbadensis) leaf juice, denatonium benzoate, fragrance, glycerin, hyaluronic acid, water

Package Label - Principal Display Panel

30 ml20ml90mlLabel 30 ml NDC 73517-111-01

Label 20 ml NDC 73517-111-02

Label 90 ml NDC 73517-111-03

OLIKA ULTRA HYDRATING HAND SANITIZER FRAGRANCE FREE 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73517-121
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73517-121-0230 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product09/01/2021
2NDC:73517-121-0320 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product09/01/2021
3NDC:73517-121-0190 mL in 1 POUCH; Type 0: Not a Combination Product09/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/30/2020
Labeler - Amyris, Inc (185930182)
Establishment
NameAddressID/FEIBusiness Operations
Taizhou Jingshang Cosmetics Technology Co., Ltd.550819554manufacture(73517-121)

Revised: 1/2023
Document Id: f3341894-02a1-0998-e053-2995a90aef68
Set id: cb0bb52c-7317-a384-e053-2995a90af3cd
Version: 3
Effective Time: 20230126
 
Amyris, Inc