SANZI DERM Antiseptic Hand Sanitizer

SANZI DERM Antiseptic Hand Sanitizer by

Drug Labeling and Warnings

SANZI DERM Antiseptic Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Beauty Partners LLC,. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SANZI DERM ANTISEPTIC HAND SANITIZER- alcohol gel 
Beauty Partners LLC,

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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SANZI DERM Antiseptic Hand Sanitizer

Drug Facts

Active ingredient

Alcohol 72%

Purpose

Antiseptic

Use(s)

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

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

Do not use

• on 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 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:

Water (Aqua), Glycerin, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Juice.

Questions?

866-961-6181

Package Labeling

SANZI DERM ANTISEPTIC HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78229-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.72 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78229-003-01	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/01/2020	08/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/01/2020	08/28/2020

Labeler - Beauty Partners LLC, (080320170)

Revised: 11/2021

Document Id: d0ffde7a-693f-74fc-e053-2a95a90a484a

34390-5

Set id: aa08625a-b8ff-bbc6-e053-2995a90a7886

Version: 2

Effective Time: 20211117