Solimo

Manufacturer: Amazon.com Services LLC | Carrollclean
Effective date: 2020-08-24
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 23:16:37

Label at a glance#

ProductSolimo

Active ingredientALCOHOL

Label structure10 sections

Indications and uses

to sanitizer hands without requiring water or a rinse help reduce bacteria that can cause disease

Dosage and administration

Apply gel liberally to unsoiled hands and rub in thoroughly. Allow to dry without wiping or rinsing.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Warnings

WARNINGS SECTION

FLAMMABLE

For external use only

In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

INSTRUCTIONS FOR USE SECTION

Apply gel liberally to unsoiled hands and rub in thoroughly.

Allow to dry without wiping or rinsing.

Other information

OTHER SAFETY INFORMATION

Store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer, Glycerin, Diidopropylamine, Isopropyl Myristate.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

When using this product

DOSAGE & ADMINISTRATION SECTION

When using this product

do not use near heat or flame
do not use in or near eyes
discontinue use if irritation and redness develop
do not use on deep or puncture wounds consulft your doctor

Uses

INDICATIONS & USAGE SECTION

to sanitizer hands without requiring water or a rinse
help reduce bacteria that can cause disease

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Products#

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

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

Solimo
70% Clear Ethanol Gel
DIISOPROPYLAMINE
ALCOHOL
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
ISOPROPYL MYRISTATE
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72288-527	72288-527-86

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
DIISOPROPYLAMINE	BR9JLI40NO	IACT
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
GLYCERIN	PDC6A3C0OX	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
ad92fb09-8784-31bd-e053-2995a90aec07			ad9317b9-af21-92de-e053-2995a90a1fc3	2020-08-24	Warnings	Exact identifier spl id: ad92fb09-8784-31bd-e053-2995a90aec07 spl set id: ad9317b9-af21-92de-e053-2995a90a1fc3

Reported adverse events (FAERS/openFDA)#

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