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

Label

SANZI DERM ANTISEPTIC HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 78229-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.72 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
TROLAMINE (UNII: 9O3K93S3TK)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 78229-003-01236 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/202008/28/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/01/202008/28/2020
Labeler - Beauty Partners LLC, (080320170)

Revised: 11/2021
 

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