Olika Ultra Hydrating Hand Sanitizer Fragrance Free

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 Ultra Hydrating Hand Sanitizer Fragrance Free
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

30 ml30 ml20ml20ml90ml90mlLabel 30 ml NDC 73517-111-01

Label 20 ml NDC 73517-111-02

Label 90 ml NDC 73517-111-03

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#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73517-121-01Olika Ultra Hydrating Hand Sanitizer Fragrance Free90 mL in 1 POUCHGEL903
73517-121-02Olika Ultra Hydrating Hand Sanitizer Fragrance Free30 mL in 1 BOTTLE, DISPENSINGGEL303
73517-121-03Olika Ultra Hydrating Hand Sanitizer Fragrance Free20 mL in 1 BOTTLE, DISPENSINGGEL203

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73517-121OLIKA ULTRA HYDRATING HAND SANITIZER FRAGRANCE FREE (ALCOHOL) GEL [AMYRIS, INC]3Legacy NDC, 3 package rows20230127_cb0bb52c-7317-a384-e053-2995a90af3cd.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73517-12173517-121-02, 73517-121-03, 73517-121-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
f3341894-02a1-0998-e053-2995a90aef68cb0bb52c-7317-a384-e053-2995a90af3cd2023-01-26WarningsExact identifier
spl id: f3341894-02a1-0998-e053-2995a90aef68
spl set id: cb0bb52c-7317-a384-e053-2995a90af3cd

Reported adverse events (FAERS/openFDA)#

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