KANGMANBABY Hand Sanitizer

Manufacturer
Zhejiang iColor Biotech Co., Ltd
Effective date
2024-01-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:12:38

Label at a glance#

ProductKANGMANBABY Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

help decrease bacteria on the hands

Dosage and administration

Dispense a small amount on palm Rub lightly until dry. Do not rinse.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

help decrease bacteria on the hands

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from heat or flame

When using this product

OTC - WHEN USING SECTION

do not use in or near eyes, ears, 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 or rash appears on the skin.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Dispense a small amount on palm
  • Rub lightly until dry.
  • Do not rinse.

Other information

SPL UNCLASSIFIED SECTION

  • Store between 15-30°C (59-86°F)
  • Avoid freezing and excessive heat above 40°C (104°F )
  • May discolor some fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Polyacrylic Acid, Aminomethyl Propanol, Fragrance, Tocopheryl Acetate, Aloe Barbadensis Leaf Extract

Package Labeling:236ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74934-050KANGMANBABY HAND SANITIZER (ALCOHOL) GEL [ZHEJIANG ICOLOR BIOTECH CO., LTD]3Legacy NDC20240125_a7d07c22-5e72-4149-91fe-5e86319edbf8.zip

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
74934-05074934-050-01, 74934-050-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
0fb3c222-c417-a7ea-e063-6394a90a24b6a7d07c22-5e72-4149-91fe-5e86319edbf82024-01-24WarningsExact identifier
spl id: 0fb3c222-c417-a7ea-e063-6394a90a24b6
spl set id: a7d07c22-5e72-4149-91fe-5e86319edbf8

Reported adverse events (FAERS/openFDA)#

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