Next Home Hand Sanitizer Gel

Manufacturer
A2A Integrated Pharmaceuticals, LLC
Effective date
2023-12-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:16:38

Label at a glance#

ProductNext Home Hand Sanitizer Gel
Active ingredientISOPROPYL ALCOHOL
Label structure10 sections

Dosage and administration

Put a small amount in palm and rub hands together briskly until dry Children under 6 years of age should be supervised when using this product

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% v/v.

PURPOSE

OTC - PURPOSE SECTION

Antimicrobial

USE

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin

WARNINGS

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and persists

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Put a small amount in palm and rub hands together briskly until dry

Children under 6 years of age should be supervised when using this product

OTHER INFORMATION

OTHER SAFETY INFORMATION

Do not store above 110°F (43°C)

May discolor certain fabrics or surfaces.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Hydroxypropyl Cellulose, Propylene Glycol, Purified Water

Questions or Comments?

INFORMATION FOR PATIENTS SECTION

Call 800-380-6709 Monday through Friday 9 AM to 5 PM

PRODUCT LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1.5 mL Label 1.5 mL Label1.5 mL Label

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73141-19073141-190-01, 73141-190-02, 73141-190-05, 73141-190-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
24b9e9c2-6c8a-4a5b-e063-6394a90a1829acc31b02-16a4-0f60-e053-2a95a90a5a7e2024-10-18WarningsExact identifier
spl set id: acc31b02-16a4-0f60-e053-2a95a90a5a7e

Reported adverse events (FAERS/openFDA)#

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