Antibacterial Hand Sanitizer

Manufacturer
Cosmuses Cosmetics (Ningbo) Co., Ltd
Effective date
2024-07-02
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:14:42

Label at a glance#

ProductAntibacterial Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Wet hands thoroughly with products and allow to dry without wiping For children under 6, use only under adult supervision Not recommended for infants

Storage and handling

Do not store above 105F May discolor some fabrics Harmful to wooden finishes and plastics

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Fact

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To decrease the bacteria on the skin that could cause disease

Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only-Hands

Flammable. Keep away from heat and flame

Stop use and ask a doctor if skin irritation develops

OTC - WHEN USING SECTION

When use this product, keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.  Do not inhale or ingest

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with products and allow to dry without wiping

For children under 6, use only under adult supervision

Not recommended for infants

Other information

STORAGE AND HANDLING SECTION

Do not store above 105F

May discolor some fabrics

Harmful to wooden finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, glycerin, propylene glycol, aloe barbadensis leaf extract, carbomer, triethanolamine, tocopheryl acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82953-00882953-008

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
247835ethanol 62 % Topical SolutionPSN4
247835ethanol 0.62 ML/ML Topical SolutionSCD4
247835ethanol 62 % Topical SolutionSY4
247835ethyl alcohol 62 % Topical SolutionSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82953-008-01Antibacterial Hand Sanitizer15 mL in 1 BOTTLESOLUTION154
82953-008-02Antibacterial Hand Sanitizer50 mL in 1 BOTTLESOLUTION504
82953-008-03Antibacterial Hand Sanitizer120 mL in 1 BOTTLESOLUTION1204
82953-008-04Antibacterial Hand Sanitizer74 mL in 1 BOTTLESOLUTION744
82953-008-05Antibacterial Hand Sanitizer0.9 mL in 1 BOTTLESOLUTION0.94

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82953-008ANTIBACTERIAL HAND SANITIZER (ALCOHOL) SOLUTION [COSMUSES COSMETICS (NINGBO) CO., LTD]4Current NDC, 5 package rows20240704_f531053d-82e4-7613-e053-2995a90a349f.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82953-00882953-008-01, 82953-008-02, 82953-008-03, 82953-008-04, 82953-008-05

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
Antibacterial Hand SanitizerALCOHOLCosmuses Cosmetics (Ningbo) Co., Ltdf531053d-82e4-7613-e053-2995a90a349f2024-07-02WarningsExact identifier
ndc (package): 82953-008-01
ndc (package): 82953-008-03
ndc (package): 82953-008-02
ndc (package): 82953-008-05
ndc (package): 82953-008-04
ndc (product): 82953-008
ndc11 (package): 82953000804
ndc11 (package): 82953000803
ndc11 (package): 82953000805
ndc11 (package): 82953000802
ndc11 (package): 82953000801
spl id: 1c3e3fea-ae9f-ff43-e063-6294a90a2a81
spl set id: f531053d-82e4-7613-e053-2995a90a349f

Reported adverse events (FAERS/openFDA)#

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