Maurices Sungari Hand Sanitizer

Maurices Sungari Hand Sanitizer by

Drug Labeling and Warnings

Maurices Sungari Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by MAURICES INCORPORATED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MAURICES SUNGARI HAND SANITIZER- alcohol gel 
MAURICES INCORPORATED

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Maurices Sungari Hand Sanitizer

Drug Facts

Active ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

• to decrease bacteria on the skin that could cause disease
• recommend for repeated use

Warnings

For external use only: hands

Flammable, keep away from fire or flame.

When using this product

• keep out of eyes. In case of contact with eyes, flush thoroughly with water
• avoid contact with broken skin
• do not inhale or ingest

Stop and ask a doctor if

• irritation and redness develop
• condition persists for more than 72 hours

Keep out of the reach of children.

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

Directions

• wet hands thoroughly with product and allow to dry without wiping
• for children under 6, use only under adult supervision
• not recommended for infants

Other Information

• do not store above 105ºF
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive Ingredients

Water/Aqua/Eau, Glycerin, PEG-7 Olivate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Aloe Barbadensis Extract, Tocopheryl Acetate, Fragrance (Parfum), Butylphenyl Methylpropional, Limonene, Hydroxycitronellal, Yellow 6 (CI 15985), Yellow 5 (CI 19140)

Package Labeling:

MAURICES SUNGARI HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80237-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PEG-7 OLEATE (UNII: 7W4ZYQ7UVQ)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80237-004-06	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/25/2020	08/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/25/2020	08/31/2022

Labeler - MAURICES INCORPORATED (053430419)

Revised: 3/2025

Document Id: 30dc2555-95c0-4257-e063-6394a90abbff

34390-5

Set id: ade086ed-34b4-85e5-e053-2995a90a2ec0

Version: 3

Effective Time: 20250321