OLIKA HYDRATING HAND SANITIZER-CLARITY- alcohol gel 
Amyris

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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OLIKA Hydrating Hand Sanitizer-Clarity

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 barbadensis leaf extract, hyaluronic acid, ganoderma lucidum (mushroom) extract, denatonium benzoate

90 ml20ml90 ML NDC# 73517-949-01

20 ML NDC# 73517-949-02

OLIKA HYDRATING HAND SANITIZER-CLARITY 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73517-949
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
HYALURONIC ACID (UNII: S270N0TRQY)  
GANODERMA LUCIDUM STEM (UNII: U8PA41532G)  
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73517-949-0190 mL in 1 POUCH; Type 0: Not a Combination Product07/29/2022
2NDC:73517-949-0220 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product07/29/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/29/2022
Labeler - Amyris (185930182)
Establishment
NameAddressID/FEIBusiness Operations
Taizhou Jingshang Cosmetics Technology Co., Ltd.550819554manufacture(73517-949)

Revised: 7/2022
Document Id: e4f727bb-f8b3-3daf-e053-2995a90ad636
Set id: e4f7192e-40a1-8aa6-e053-2995a90ad1ca
Version: 1
Effective Time: 20220729
 
Amyris