FDA.reportPublic FDA data

OLIKA Ultra Hydrating Hand Sanitizer, Bold

Manufacturer
Amyris, Inc | Taizhou Jingshang Cosmetics Technology Co., Ltd.
Effective date
2022-05-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:49:30

Label at a glance#

ProductOLIKA Ultra Hydrating Hand Sanitizer, Bold
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 vera (aloe barbadensis) leaf juice, hyaluronic acid, denatonium benzoate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

90 ml pouch90 ml pouchboldbold

NDC: 73517-921-02 0.6 OZ

NDC: 73517-921-03 3 OZ

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
902515ethanol 65 % Topical SprayPSN2
902515ethanol 0.65 ML/ML Topical SpraySCD2
902515ethanol 65 % Topical SpraySY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73517-921-022024-01-30C16284748780-11030e365-67e2-111a-e063-dadaa90a10e2OLIKA Ultra Hydrating Hand Sanitizer, Bold
73517-921-032024-01-30C16284748780-11030e365-67e2-111a-e063-dadaa90a10e2OLIKA Ultra Hydrating Hand Sanitizer, Bold

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73517-921-02OLIKA Ultra Hydrating Hand Sanitizer, Bold20 mL in 1 BOTTLE, DISPENSINGGEL202
73517-921-03OLIKA Ultra Hydrating Hand Sanitizer, Bold90 mL in 1 BOTTLE, DISPENSINGGEL902

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73517-921OLIKA ULTRA HYDRATING HAND SANITIZER, BOLD (ALCOHOL) GEL [AMYRIS, INC]2Legacy NDC, 2 package rows20220509_de602bc7-79b5-2a30-e053-2a95a90afa2a.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73517-92173517-921-02, 73517-921-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
FRAGRANCE 135765EM498GW35IACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
DENATONIUM BENZOATE4YK5Z54AT2IACT
ALCOHOL3K9958V90MACTIB
HYALURONATE SODIUMYSE9PPT4THIACT

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
de787fa0-b965-54d9-e053-2a95a90a9576de602bc7-79b5-2a30-e053-2a95a90afa2a2022-05-07WarningsExact identifier
spl id: de787fa0-b965-54d9-e053-2a95a90a9576
spl set id: de602bc7-79b5-2a30-e053-2a95a90afa2a

Reported adverse events (FAERS/openFDA)#

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