antibacterial hand sanitizer spray

Manufacturer
Cosmuses Cosmetics (Ningbo) Co., Ltd.
Effective date
2024-05-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:13:07

Label at a glance#

Producthand sanitizer 01
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

For hand Sanitizing

Dosage and administration

Wet hands throughly with product and allow to dry without wiping. For children under 6 age use only under adult supervision. Not recommended for infants.

Storage and handling

Other information ​ Do not store above 105 o F. May discolor some fabrics.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For hand Sanitizing

Warnings

WARNINGS SECTION

For external use only- hands.

Flammable. Keep away from heat and flame.

OTC - WHEN USING SECTION

When using 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 - STOP USE SECTION

Stop use and ask doctor if skin irritation develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands throughly with product and allow to dry without wiping.
  • For children under 6 age use only under adult supervision.
  • Not recommended for infants.

STORAGE AND HANDLING SECTION

Other information ​

  • Do not store above 105 oF.
  • May discolor some fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua, Glycerin, Propylene Glycol, Aloe Barbadensis Leaf Extract, Carbomer, Triethanolamine, Tocopheryl Acetate, Fragrance, PEG-40 Hydrogenated Castor Oil.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82953-01582953-015

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
247835ethanol 62 % Topical SolutionPSN1
247835ethanol 0.62 ML/ML Topical SolutionSCD1
247835ethanol 62 % Topical SolutionSY1
247835ethyl alcohol 62 % Topical SolutionSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82953-015-01hand sanitizer0110 mL in 1 BOTTLE, PLASTICLIQUID101
82953-015-02hand sanitizer0120 mL in 1 BOTTLE, PLASTICLIQUID201
82953-015-03hand sanitizer0125 mL in 1 BOTTLE, PLASTICLIQUID251
82953-015-04hand sanitizer0115 mL in 1 BOTTLE, PLASTICLIQUID151
82953-015-05hand sanitizer018 mL in 1 BOTTLE, PLASTICLIQUID81
82953-015-06hand sanitizer0118 mL in 1 BOTTLE, PLASTICLIQUID181
82953-015-07hand sanitizer015 mL in 1 BOTTLE, PLASTICLIQUID51
82953-015-08hand sanitizer0130 mL in 1 BOTTLE, PLASTICLIQUID301
82953-015-09hand sanitizer0160 mL in 1 BOTTLE, PLASTICLIQUID601
82953-015-10hand sanitizer0190 mL in 1 BOTTLE, PLASTICLIQUID901

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82953-015HAND SANITIZER 01 (ALCOHOL) LIQUID [COSMUSES COSMETICS (NINGBO) CO., LTD.]1Current NDC, 10 package rows20240531_19a6c3c6-4b27-9011-e063-6394a90ae512.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
hand sanitizer 01ALCOHOLCosmuses Cosmetics (Ningbo) Co., Ltd.19a6c3c6-4b27-9011-e063-6394a90ae5122024-05-30WarningsExact identifier
ndc (package): 82953-015-01
ndc (package): 82953-015-05
ndc (package): 82953-015-09
ndc (package): 82953-015-02
ndc (package): 82953-015-04
ndc (package): 82953-015-10
ndc (package): 82953-015-03
ndc (package): 82953-015-07
ndc (package): 82953-015-06
ndc (package): 82953-015-08
ndc (product): 82953-015
ndc11 (package): 82953001505
ndc11 (package): 82953001509
ndc11 (package): 82953001510
ndc11 (package): 82953001508
ndc11 (package): 82953001506
ndc11 (package): 82953001503
ndc11 (package): 82953001504
ndc11 (package): 82953001501
ndc11 (package): 82953001507
ndc11 (package): 82953001502
spl id: 19a6dd5a-38d8-2768-e063-6294a90a3909
spl set id: 19a6c3c6-4b27-9011-e063-6394a90ae512

Reported adverse events (FAERS/openFDA)#

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