FDA.reportPublic FDA data

OLIKA Hydrating Hand Sanitizer, Sandalwood

Manufacturer
Amyris, Inc | Taizhou Jingshang Cosmetics Technology Co., Ltd.
Effective date
2022-07-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:50:18

Label at a glance#

ProductOLIKA Hydrating Hand Sanitizer, Sandalwood
Active ingredientALCOHOL
Label structure12 sections

Storage and handling

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

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65% v/v. Purpose: Antiseptic

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

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

OTC - DO NOT USE SECTION

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

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

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.

STORAGE AND HANDLING SECTION

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

INACTIVE INGREDIENT SECTION

water, glycerin, fragrance, aloe barbadensis leaf extract, hyaluronic acid, ganoderma lucidum (mushroom) extract, denatonium benzoate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

20 mL 73517-737-02

90 mL 73517-737-01 90 ml90 ml 20ml20ml

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73517-737-012024-01-30C16284748780-11030e365-542a-111a-e063-dadaa90a10e2OLIKA Hydrating Hand Sanitizer- Sandalwood
73517-737-022024-01-30C16284748780-11030e365-542a-111a-e063-dadaa90a10e2OLIKA Hydrating Hand Sanitizer- Sandalwood

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73517-737-01OLIKA Hydrating Hand Sanitizer, Sandalwood90 mL in 1 POUCHGEL901
73517-737-02OLIKA Hydrating Hand Sanitizer, Sandalwood20 mL in 1 BOTTLE, DISPENSINGGEL201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73517-737OLIKA HYDRATING HAND SANITIZER, SANDALWOOD (ALCOHOL) GEL [AMYRIS, INC]1Legacy NDC, 2 package rows20220731_e4d32298-7e78-f954-e053-2995a90a6acc.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73517-73773517-737-01, 73517-737-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
GANODERMA LUCIDUM STEMU8PA41532GIACT
ALOE VERA LEAFZY81Z83H0XIACT
HYALURONIC ACIDS270N0TRQYIACT
GLYCERINPDC6A3C0OXIACT
DENATONIUM BENZOATE4YK5Z54AT2IACT
WATER059QF0KO0RIACT
FRAGRANCE 135765EM498GW35IACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e4d322f2-495b-086b-e053-2a95a90ae796e4d32298-7e78-f954-e053-2995a90a6acc2022-07-27WarningsExact identifier
spl id: e4d322f2-495b-086b-e053-2a95a90ae796
spl set id: e4d32298-7e78-f954-e053-2995a90a6acc

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.