SKINAPPLE HAND SANITIZER gel

Manufacturer
Rainbow Co Ltd
Effective date
2020-04-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:05:31

Label at a glance#

ProductSKINAPPLE HAND SANITIZER gel
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ethyl alcohol

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, dipropylene glycol, triethaneolamine, peg-60 hydrogenated castor oil, panthenol, camellia sinensis leaf extract, diethanolamine, grapefruit peel oil

OTC - PURPOSE SECTION

to desrease bacteria on hands.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.

Supervise children in the use of this product.

WARNINGS SECTION

■ Flammable. Keep away from fire or flame.

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74247-0003-12021-07-23C16284748780-1c7ccaba7-250e-fd44-e053-dadaa90aa01bDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74247-0003-1SKINAPPLE HAND SANITIZER gel500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74247-0003SKINAPPLE HAND SANITIZER GEL (ALCOHOL) GEL [RAINBOW CO LTD]1Legacy NDC, 1 package rows20200409_a2c28ab8-f9d3-ef92-e053-2995a90abddb.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
74247-000374247-0003-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
a2c28ab5-2693-c142-e053-2995a90a7cd6a2c28ab8-f9d3-ef92-e053-2995a90abddb2020-04-08WarningsExact identifier
spl id: a2c28ab5-2693-c142-e053-2995a90a7cd6
spl set id: a2c28ab8-f9d3-ef92-e053-2995a90abddb

Reported adverse events (FAERS/openFDA)#

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