TinMeZor Hand Sanitizer by Guangzhou Danting Bath&Body Care Industry Co. Ltd. TinMeZor Hand Sanitizer

TinMeZor Hand Sanitizer by

Drug Labeling and Warnings

TinMeZor Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Guangzhou Danting Bath&Body Care Industry Co. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

TINMEZOR HAND SANITIZER- alcohol gel 
Guangzhou Danting Bath&Body Care Industry Co. Ltd.

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TinMeZor Hand Sanitizer

Drug Facts

Active ingredient[s]

Alcohol 75% v/v

Purpose

Antiseptic

Use[s]

Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

Warnings

For external use only. Flammable.

Keep away from heat or flame

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product

keep out of 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 occurs. These may be signs of a serious condition.

Keep out of reach of children.

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

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Pure water, Triethanolamine, Carbomer, Glycerin, Fragrance, Benzalkonium chloride

Package Labeling:

TINMEZOR HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75376-006
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)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75376-006-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/10/2020	07/23/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/10/2020	07/23/2023

Labeler - Guangzhou Danting Bath&Body Care Industry Co. Ltd. (545337886)

Revised: 5/2025

Document Id: 3509ceda-c378-1b80-e063-6294a90ade6d

34390-5

Set id: b4c9236b-2b51-4ae9-9ed9-a10e1749b361

Version: 3

Effective Time: 20250513

 

Guangzhou Dant