Safe Choice Hand Sanitizer

Manufacturer
Aquagenics Technologies | Precision Medical Devices
Effective date
2023-07-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:28:08

Label at a glance#

ProductSafe Choice Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Apply product onto hands, briskly rub hands together until dry without wiping. For children under 6, use only under adult supervision.

Storage and handling

Store at a temperature below 110F (43C)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65% Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on skin.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame.

OTC - WHEN USING SECTION

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Avoid contact with eyes. In case of contact, flush thoroughly with water. Do not inhale or ingest. Avoid contact with broken skin.

Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

OTC - STOP USE SECTION

Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply product onto hands, briskly rub hands together until dry without wiping. For children under 6, use only under adult supervision.

Other information

STORAGE AND HANDLING SECTION

Store at a temperature below 110F (43C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water, glycerin, carbomer, aloe, fragrance.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

236 mL NDC: 73763-365-01

front panelfront panel

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73763-36573763-365-01, 73763-365-02, 73763-365-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
28631f76-3d4d-2235-e063-6394a90aef4ea9c83c82-a138-cb96-e053-2a95a90a3e932024-12-03WarningsExact identifier
spl set id: a9c83c82-a138-cb96-e053-2a95a90a3e93

Reported adverse events (FAERS/openFDA)#

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