KANGMANBABY Hand Sanitizer

KANGMANBABY Hand Sanitizer by

Drug Labeling and Warnings

KANGMANBABY Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Zhejiang iColor Biotech Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

KANGMANBABY HAND SANITIZER- alcohol gel 
Zhejiang iColor Biotech Co., Ltd

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KANGMANBABY Hand Sanitizer

Drug Facts

Active ingredient

Ethyl Alcohol 75% v/v

Purpose

Antiseptic

Uses

help decrease bacteria on the hands

Warnings

For external use only.

Flammable. Keep away from heat or flame

When using this product

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

if irritation or rash appears on the skin.

Keep out of reach of children.

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

Directions

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

Other information

• 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

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

Package Labeling:236ml

Package Labeling:500ml

KANGMANBABY HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74934-050
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74934-050-01	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/28/2020	01/31/2026
2	NDC: 74934-050-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/28/2020	01/31/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/28/2020	01/31/2026

Labeler - Zhejiang iColor Biotech Co., Ltd (554528308)

Revised: 1/2024

Document Id: 0fb3c222-c417-a7ea-e063-6394a90a24b6

34390-5

Set id: a7d07c22-5e72-4149-91fe-5e86319edbf8

Version: 3

Effective Time: 20240124