SOLGREAT ALCOHOL-FREE HAND SANITIZER- benzalkonium chloride gel

SolGreat Alcohol-Free Hand Sanitizer by

Drug Labeling and Warnings

SolGreat Alcohol-Free Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by PANATURAL USA, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active lngredient  

Benzalkonium Chloride

Purpose 

Antibacterial

Uses

• hand sanitizer to help decrease bacteria on the skin, when water, soap & towel are not available.
• recommended for repeated use

Warnings  

For external use only.

Flammable. Keep away from fire or flame.

Do not apply around eyes. Do not use in ears & mouth.

When using this product, avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

Directions

• place enough product into your palms and thoroughly spread on both hands.
• rub into skin until dry.

Inactive ingredients 

BUTYLENE GLYCOL, CITRIC ACID, DIAZOLIDINYL UREA, HYDROXYETHYCELLULOSE, PEG-40 HYDROGENATE CASTOR OIL, PROPYLENE GLYCOL, WATER.

Keep out of reach of children

Children must be supervised in use of this product

Products Label-237mL SolGreat Alcohol-Free Hand Sanitizer

Product Label- 500mL SolGreat Alcohol-Free Hand Sanitizer

INGREDIENTS AND APPEARANCE

SOLGREAT ALCOHOL-FREE HAND SANITIZER 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73913-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73913-004-01	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/27/2020
2	NDC: 73913-004-02	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/23/2020

Labeler - PANATURAL USA, INC. (029572239)

Establishment
Name	Address	ID/FEI	Business Operations
Hefei Yatai Daily-Use Chemical Industry Co., Ltd		654641724	manufacture(73913-004)