GLOW HANDS ON SANITIZER

Manufacturer
Sinbad Co.,Ltd | CAREPHARM
Effective date
2020-05-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:14:42

Label at a glance#

ProductGLOW HANDS ON SANITIZER
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

Hand sanitizer to help reduce bacteria on skin.

Dosage and administration

Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70.0% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

DOSAGE & ADMINISTRATION SECTION

Hand sanitizer to help reduce bacteria on skin.

Warnings

WARNINGS SECTION

For extrnal use only. Flammable. Keep away from heat or flame.

OTC - WHEN USING SECTION

When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask doctor if iffitation or rash appears and lasts.

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 right away.

Directions:

INDICATIONS & USAGE SECTION

  • Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.
  • Children under 6 years of age should be supervised when using this product.

Other Information:

OTHER SAFETY INFORMATION

  • Store below 106°F. (41°C)
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Carbomer, Aloe Barbadensis Leaf Juice, Glycerin, Tocopherol, Triethanolamine, Propylene Glycol, FD&C Blue No.1, FD&C Yellow No.5

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50mL Label50mL Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74142-301-102022-01-28C16284748780-1d6a99b39-8d30-a426-e053-dadaa90af4c2a3defdd6-3b67-a2ae-e053-2a95a90a681f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74142-301-10GLOW HANDS ON SANITIZER50 mL in 1 BOTTLEGEL502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74142-301GLOW HANDS ON SANITIZER (HAND SANITIZER) GEL [SINBAD CO.,LTD]2Legacy NDC, 1 package rows20200527_a3defdd6-3b67-a2ae-e053-2a95a90a681f.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74142-30174142-301-10

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
a68538e1-6035-dcec-e053-2a95a90ad572a3defdd6-3b67-a2ae-e053-2a95a90a681f2020-05-25WarningsExact identifier
spl id: a68538e1-6035-dcec-e053-2a95a90ad572
spl set id: a3defdd6-3b67-a2ae-e053-2a95a90a681f

Reported adverse events (FAERS/openFDA)#

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