Aura Cacia Hand Sanitizer

Manufacturer
Frontier Co-op | Aura Cacia
Effective date
2023-12-20
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:17:30

Label at a glance#

ProductAura Cacia Hand Sanitizer Unscented
Active ingredientALCOHOL
Label structure11 sections

Storage and handling

Other information Store between 15°-30°C (59°-86°F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Alcohol 80% v/v

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Uses

  • for hand washing to decrease bacteria on the skin
  • recommended for repeated use

WARNINGS SECTION

Warnings

For external use only

Flammable. Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product avoid contact with the eyes. In case of contact, flush eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop or persist for more than 72 hours.

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.

DOSAGE & ADMINISTRATION SECTION

Directions

  • wet hands thoroughly with product
  • allow to dry without wiping
  • supervise children under 6 years old
  • not recommended for infants

STORAGE AND HANDLING SECTION

Other information

  • Store between 15°-30°C (59°-86°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients

Purified water USP, glycerin, hydrogen peroxide.

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY FRONTIER CO-OP

NORWAY, IA 52318 USA

1-800-669-3275

©2020 FRONTIER CO-OP

WWW.AURACACIA.COM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AURA CACIA®

HAND SANITIZER

Non-sterile Solution

UNSCENTED

Alcohol Antiseptic 80% Topical Solution

Kills 99.9% of Common Germs

2 FL OZ (59 mL)

UNSCENTED 2 FL OZUNSCENTED 2 FL OZ

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74246-10474246-104-02

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
0cf79b4d-c1c2-2268-e063-6294a90a1239a7cf1567-1bdb-b2a0-e053-2995a90a7c8a2023-12-20WarningsExact identifier
spl id: 0cf79b4d-c1c2-2268-e063-6294a90a1239
spl set id: a7cf1567-1bdb-b2a0-e053-2995a90a7c8a

Reported adverse events (FAERS/openFDA)#

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