Roni, Hand Sanitizer, Ethyl Alcohol 67% w/w, Gel, 59mL

Manufacturer
Ningbo Roni Cosmetic Co., Ltd | A03 Lab of BTS
Effective date
2020-05-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:11:03

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Dispense product evenly on palms or on material surface and rub your hands until dry. Children should be under adult supervision when using this product. No dilute required.

Storage and handling

Store at 20℃ to 25℃.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 67% w/w. Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial.

Use

INDICATIONS & USAGE SECTION

Uses for handwashing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from heat and flame.

Do not use

OTC - DO NOT USE SECTION

Do not us in the eyes. In case of contact, rinse eyes troroughly with water.

OTC - WHEN USING SECTION

When using this product, do not use in or near the eyes or wound.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

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

  • Dispense product evenly on palms or on material surface and rub your hands until dry.
  • Children should be under adult supervision when using this product.
  • No dilute required.

Other information

STORAGE AND HANDLING SECTION

Store at 20℃ to 25℃.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Carbomer, Triethanolamine, Aloe barbadensis leaf juice, Tocopherol, Fragrance.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5959

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77309-101-172022-01-28C16284748780-1d6a99b39-710a-a426-e053-dadaa90af4c2Roni, Hand Sanitizer, Ethyl Alcohol 67% w/w, Gel, 59mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77309-101-01Hand Sanitizer59 mL in 1 BOTTLEGEL591
77309-101-17Hand Sanitizer200 in 1 CARTONGEL2001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77309-101HAND SANITIZER (ALCOHOL) GEL [NINGBO RONI COSMETIC CO., LTD]1Legacy NDC, 2 package rows20200513_a576c6cb-9bba-1832-e053-2995a90a45e9.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77309-10177309-101-01, 77309-101-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML · Source PDF

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
a576c6cb-9bbb-1832-e053-2995a90a45e9a576c6cb-9bba-1832-e053-2995a90a45e92020-05-12WarningsExact identifier
spl id: a576c6cb-9bbb-1832-e053-2995a90a45e9
spl set id: a576c6cb-9bba-1832-e053-2995a90a45e9

Reported adverse events (FAERS/openFDA)#

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