FDA.reportPublic FDA data

White Cloud Hand Sanitizer

Manufacturer
Moderplas, S. de R.L. de C.V.
Effective date
2020-10-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:13:12

Label at a glance#

ProductWhite Cloud Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Put product on your hands and rub together and between fingers until dry. Children undre 6 years old, use under adult supervision.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • Hand sanitizer to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Flammable, Keep away fire or flame.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. In case of contact with eyes, rinse thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

If irritation or rash develop and persists.

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

  • Put product on your hands and rub together and between fingers until dry.
  • Children undre 6 years old, use under adult supervision.

Other information

SPL UNCLASSIFIED SECTION

  • Do not store above 105°F, may discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, carbomers, glycerin, aloe vera, hydrogen peroxide.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80477-001-002022-03-16C16284748780-1d6a99b39-47a1-a426-e053-dadaa90af4c2White Cloud Hand Sanitizer
80477-001-002022-01-28C16284748780-1d6a99b39-47a1-a426-e053-dadaa90af4c2White Cloud Hand Sanitizer

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80477-00180477-001-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
ALCOHOL3K9958V90MACTIB

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
da5646b6-b597-f6f1-e053-2a95a90ad309aefc0ce6-2b1a-205d-e053-2a95a90a6c1c2022-03-16WarningsExact identifier
spl set id: aefc0ce6-2b1a-205d-e053-2a95a90a6c1c

Reported adverse events (FAERS/openFDA)#

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