OLIKA ULTRA HYDRATING HAND SANITIZER, BOLD- 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.

----------

OLIKA Ultra Hydrating Hand Sanitizer, Bold

Ethyl Alcohol 65% v/v. Purpose: Antiseptic

Antiseptic, Hand Sanitizer

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

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

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

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.

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.

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

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

90 ml pouchbold

NDC: 73517-921-02 0.6 OZ

NDC: 73517-921-03 3 OZ

OLIKA ULTRA HYDRATING HAND SANITIZER, BOLD 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73517-921
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
FRAGRANCE 13576 (UNII: 5EM498GW35)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73517-921-0220 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/09/2022
2NDC:73517-921-0390 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/09/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/09/2022
Labeler - Amyris, Inc (185930182)
Establishment
NameAddressID/FEIBusiness Operations
Taizhou Jingshang Cosmetics Technology Co., Ltd.550819554manufacture(73517-921)

Revised: 5/2022
Document Id: de787fa0-b965-54d9-e053-2a95a90a9576
Set id: de602bc7-79b5-2a30-e053-2a95a90afa2a
Version: 2
Effective Time: 20220507
 
Amyris, Inc