SolGreat by PANATURAL USA, INC. SOLGREAT- alcohol gel

SolGreat by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient

Alcohol 70% v/v.

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

• in 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

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 15-300C (59-860F)
• Avoid freezing and excessive heat above 400C (1040F)

Inactive ingredients

aminomethyl propanol, carbomer, glycerin, hydrogen peroxide, purified water USP, tocopheryl acetate.

Package Label - Principal Display Panel

60 mL

237 mL

500 mL

1000 mL

3785 mL

1000000 mL

INGREDIENTS AND APPEARANCE

SOLGREAT 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73913-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73913-008-01	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/08/2020
2	NDC: 73913-008-02	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/08/2020
3	NDC: 73913-008-03	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/08/2020
4	NDC: 73913-008-04	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/08/2020
5	NDC: 73913-008-05	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/08/2020
6	NDC: 73913-008-06	1000000 mL in 1 TANK; 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 - PANATURAL USA, INC. (029572239)