CLOUD9 HAND SANITIZER S

Manufacturer
COSNINE Inc | COSNINE, INC.
Effective date
2020-04-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:07:59

Label at a glance#

ProductCLOUD9 HAND SANITIZER S
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

Hand sanitizer to help reduce bacteria on hands. Recommended for repeated use.

Dosage and administration

Apply a small amount onto hands and rub briskly until dry. Supervise children in the use of this product.

Storage and handling

Store at 15-30ºC (59-86ºF) Avoid freezing and excessive heat above 40 º C (104ºF)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 80%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on hands.
Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable - Keep away from fire or flame

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes, ear and mouth.
  • In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation and redness develop or increase.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply a small amount onto hands and rub briskly until dry.
  • Supervise children in the use of this product.

Other information

STORAGE AND HANDLING SECTION

  • Store at 15-30ºC (59-86ºF)
  • Avoid freezing and excessive heat above 40 ºC (104ºF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Hydrogen Peroxide

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500 mL NDC: 73330-0012-1

500ml label500ml label

100 mL NDC: 73330-0012-2

100ml label100ml label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1241663ethanol 80 % Topical SprayPSN1
1241663ethanol 0.8 ML/ML Topical SpraySCD1
1241663ethanol 80 % Topical SpraySY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73330-0013-12022-01-28C16284748780-1d6a99b39-be75-a426-e053-dadaa90af4c2a41b3de5-e062-75f2-e053-2a95a90aa6e4
73330-0013-22022-01-28C16284748780-1d6a99b39-be75-a426-e053-dadaa90af4c2a41b3de5-e062-75f2-e053-2a95a90aa6e4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73330-0013-1CLOUD9 HAND SANITIZER S500 mL in 1 BOTTLE, SPRAYLIQUID5001
73330-0013-2CLOUD9 HAND SANITIZER S100 mL in 1 BOTTLE, SPRAYLIQUID1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73330-0013CLOUD9 HAND SANITIZER S (ETHYL ALCOHOL) LIQUID [COSNINE INC]1Legacy NDC, 2 package rows20200426_a41b3de5-e062-75f2-e053-2a95a90aa6e4.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
73330-001373330-0013-1, 73330-0013-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
a41b4084-9c8b-8d72-e053-2995a90a32f1a41b3de5-e062-75f2-e053-2a95a90aa6e42020-04-25WarningsExact identifier
spl id: a41b4084-9c8b-8d72-e053-2995a90a32f1
spl set id: a41b3de5-e062-75f2-e053-2a95a90aa6e4

Reported adverse events (FAERS/openFDA)#

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