SolGreat

Manufacturer: PANATURAL USA, INC.
Effective date: 2020-06-08
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:17:40

Label at a glance#

ProductSolGreat

Active ingredientALCOHOL

Label structure9 sections

Dosage and administration

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.

Storage and handling

Store between 15-30 0 C (59-86 0 F) Avoid freezing and excessive heat above 40 0 C (104 0 F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 mL

237 mL

500 mL

1000 mL

3785 mL

1000000 mL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
5eb9f24b-9328-475e-af0a-18021935eb6a	Product name	1	20180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73913-008-01	2022-01-28	C162847	48780-1	d6a99b39-f52a-a426-e053-dadaa90af4c2	8b9395fe-4083-4b47-994f-8a2b753f1824
73913-008-02	2022-01-28	C162847	48780-1	d6a99b39-f52a-a426-e053-dadaa90af4c2	8b9395fe-4083-4b47-994f-8a2b753f1824
73913-008-03	2022-01-28	C162847	48780-1	d6a99b39-f52a-a426-e053-dadaa90af4c2	8b9395fe-4083-4b47-994f-8a2b753f1824
73913-008-04	2022-01-28	C162847	48780-1	d6a99b39-f52a-a426-e053-dadaa90af4c2	8b9395fe-4083-4b47-994f-8a2b753f1824
73913-008-05	2022-01-28	C162847	48780-1	d6a99b39-f52a-a426-e053-dadaa90af4c2	8b9395fe-4083-4b47-994f-8a2b753f1824
73913-008-06	2022-01-28	C162847	48780-1	d6a99b39-f52a-a426-e053-dadaa90af4c2	8b9395fe-4083-4b47-994f-8a2b753f1824

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
73913-008-01	SolGreat	60 mL in 1 BOTTLE, PLASTIC	GEL	60	1
73913-008-02	SolGreat	237 mL in 1 BOTTLE, PLASTIC	GEL	237	1
73913-008-03	SolGreat	500 mL in 1 BOTTLE, PLASTIC	GEL	500	1
73913-008-04	SolGreat	1000 mL in 1 BOTTLE, PLASTIC	GEL	1000	1
73913-008-05	SolGreat	3785 mL in 1 BOTTLE, PLASTIC	GEL	3785	1
73913-008-06	SolGreat	1000000 mL in 1 TANK	GEL	1000000	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73913-008	SOLGREAT (ALCOHOL) GEL [PANATURAL USA, INC.]	1	Legacy NDC, 6 package rows	20200615_8b9395fe-4083-4b47-994f-8a2b753f1824.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

SolGreat
Alcohol
AMINOMETHYLPROPANOL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
GLYCERIN
HYDROGEN PEROXIDE
.ALPHA.-TOCOPHEROL ACETATE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73913-008	73913-008-01, 73913-008-02, 73913-008-03, 73913-008-04, 73913-008-05, 73913-008-06

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
GLYCERIN	PDC6A3C0OX	IACT
HYDROGEN PEROXIDE	BBX060AN9V	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
WATER	059QF0KO0R	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
241d00e5-5c3a-4d3f-bb18-4777d0fcefcc			8b9395fe-4083-4b47-994f-8a2b753f1824	2020-06-08	Warnings	Exact identifier spl id: 241d00e5-5c3a-4d3f-bb18-4777d0fcefcc spl set id: 8b9395fe-4083-4b47-994f-8a2b753f1824

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.