Rosario Bendek hand sanitizer

Manufacturer
Zhejiang Meizhiyuan Cosmetics Co., Ltd | Townley Inc.
Effective date
2020-05-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:33:06

Label at a glance#

ProductRosario Bendek hand sanitizer 01
Active ingredientALCOHOL
Label structure13 sections

Label contents#

Full prescribing information#

DRUG FACTS

DESCRIPTION SECTION

Kills 99.9% of germs

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient ...............................Purpose

Ethanol (Alcohol) 70%- 75% v/v .......antimicrobial

use

OTC - PURPOSE SECTION

Hand sanitizer to helo reduce bacteria on skin.

WARNINGS SECTION

Flamable.Keep away from fire or flame.

For external use only.

PRECAUTIONS SECTION

Do not ingest, If swallowed seek medical help.

OTC - WHEN USING SECTION

Avoid contact with eyes.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - STOP USE SECTION

Children under 6 years old to use under adult supervision, incase of irritation, discontinue use and consult your doctor.

INDICATIONS & USAGE SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

Apply gel on hands and rub gently for 20 seconds until product evaporates.

Other information

OTHER SAFETY INFORMATION

Store below 106 oF(41 oC). May discolor certain fabric or surfaces.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Ethyl Alcohol, Aqua (Deionizer water), Glycerin, Propylene Glycol, Aloe Barbadensis (Aloe Vera) gel, Carbomer, Triethanolamine, Tocophenyl Acetate (Vitamin E), Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

54304-057-0154304-057-01

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54304-05754304-057-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
aa77004c-1cf9-151b-e053-2995a90a5475a49f9a31-bec2-5d92-e053-2995a90a4a762020-07-15WarningsExact identifier
spl set id: a49f9a31-bec2-5d92-e053-2995a90a4a76

Reported adverse events (FAERS/openFDA)#

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