SANXIDERM ANTI-BACTERIAL HAND GEL 8OZ- alcohol gel SANZIDERM ANTISEPTIC HAND SANITIZER 8OZ- alcohol gel

SANZIDERM Antiseptic Hand Sanitizer 8OZ by

Drug Labeling and Warnings

SANZIDERM Antiseptic Hand Sanitizer 8OZ by is a Otc medication manufactured, distributed, or labeled by Beauty Partners LLC, Nu-World Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
2. Glycerol (1.45% v/v).
3. Hydrogen peroxide (0.125% v/v).
4. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

Alcohol 72% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

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

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

WHEN USING

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.

STOP USE

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

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

Water, Carbomer, Aminomethyl Propanol,Butylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice, Isopropyl Myristate, Ethyl Hexanediol, Phenoxyethanol

Package Label - Principal Display Panel-SANXIDERM Anti-bacterial Hand Gel

236mL NDC: 78229-001-00

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL-SANZIDERM Antiseptic Hand Sanitizer 8OZ

236ML NDC: 78229-002-00

INGREDIENTS AND APPEARANCE

SANXIDERM ANTI-BACTERIAL HAND GEL 8OZ 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78229-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	72 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.01 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	27.65597 mL  in 100 mL
ETHOHEXADIOL (UNII: M9JGK7U88V)	0.00015 mL  in 100 mL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)	0.25 mL  in 100 mL
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)	0.01 mL  in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0098 mL  in 100 mL
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)	0.001 mL  in 100 mL
PHENOXYETHANOL (UNII: HIE492ZZ3T)	0.00005 mL  in 100 mL
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)	0.06303 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78229-001-00	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/08/2020

SANZIDERM ANTISEPTIC HAND SANITIZER 8OZ 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78229-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	72 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.01 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	27.65597 mL  in 100 mL
ETHOHEXADIOL (UNII: M9JGK7U88V)	0.00015 mL  in 100 mL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)	0.25 mL  in 100 mL
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)	0.01 mL  in 100 mL
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.0098 mL  in 100 mL
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)	0.001 mL  in 100 mL
PHENOXYETHANOL (UNII: HIE492ZZ3T)	0.00005 mL  in 100 mL
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)	0.06303 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78229-002-00	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/08/2020

Labeler - Beauty Partners LLC (080320170)

Registrant - Nu-World Corporation (628045858)

Establishment
Name	Address	ID/FEI	Business Operations
Nu-World Corporation		628045858	manufacture(78229-001, 78229-002)