FDA.reportPublic FDA data

OLIKA Hydrating Hand Sanitizer- Mint Citrus

Manufacturer
Amyris, Inc | Taizhou Jingshang Cosmetics Technology Co., Ltd.
Effective date
2023-01-26
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:53:30

Label at a glance#

ProductOLIKA Hydrating Hand Sanitizer- Mint Citrus
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

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

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

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 65% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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

Do not use

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.
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.

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.

Directions

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.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

20 mL NDC: 73517-353-06

30 mL NDC: 73517-353-05

90 mL NDC: 73517-353-04 mint citrus 90 mlmint citrus 90 ml mint citrus 20 mlmint citrus 20 ml mint citrus 30 mlmint citrus 30 ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
902515ethanol 65 % Topical SprayPSN3
902515ethanol 0.65 ML/ML Topical SpraySCD3
902515ethanol 65 % Topical SpraySY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73517-353-042025-01-30C16284748780-12cef2736-908d-d83d-e063-dadaa90ab31fOLIKA Hydrating Hand Sanitizer- Mint Citrus
73517-353-052025-01-30C16284748780-12cef2736-908d-d83d-e063-dadaa90ab31fOLIKA Hydrating Hand Sanitizer- Mint Citrus
73517-353-062025-01-30C16284748780-12cef2736-908d-d83d-e063-dadaa90ab31fOLIKA Hydrating Hand Sanitizer- Mint Citrus

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73517-353-04OLIKA Hydrating Hand Sanitizer- Mint Citrus90 mL in 1 POUCHGEL903
73517-353-05OLIKA Hydrating Hand Sanitizer- Mint Citrus30 mL in 1 BOTTLE, DISPENSINGGEL303
73517-353-06OLIKA Hydrating Hand Sanitizer- Mint Citrus20 mL in 1 BOTTLE, DISPENSINGGEL203

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73517-353OLIKA HYDRATING HAND SANITIZER- MINT CITRUS (ALCOHOL) GEL [AMYRIS, INC]3Legacy NDC, 3 package rows20230127_cb0b627a-1a11-ee10-e053-2995a90afe9d.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
73517-35373517-353-05, 73517-353-06, 73517-353-04

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
HYALURONATE SODIUMYSE9PPT4THIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
FRAGRANCE MINT ORC2000774G7LK3FFB99IACT

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
f3343345-b939-9319-e053-2995a90ab104cb0b627a-1a11-ee10-e053-2995a90afe9d2023-01-26WarningsExact identifier
spl id: f3343345-b939-9319-e053-2995a90ab104
spl set id: cb0b627a-1a11-ee10-e053-2995a90afe9d

Reported adverse events (FAERS/openFDA)#

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