FDA.reportPublic FDA data

Hand Sanitizer with Aloe

Manufacturer
Rustic Root Soap LLC
Effective date
2023-01-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:42:06

Label at a glance#

ProductHand Sanitizer with Aloe
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Isopropyl Alcohol 60.67% v/v……….....Antiseptic

OTC - PURPOSE SECTION

Active Ingredient Purpose

Isopropyl Alcohol 60.67% v/v……….....Antiseptic

INDICATIONS & USAGE SECTION

Uses

  • To decrease bacteria on the skin that could cause disease.
  • Recommended for repeated use.

WARNINGS SECTION

Warnings

For external use only.

Flammable. Keep away from heat and flame.

When using this product:

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

Stop use and ask a doctor if skin irritation develops.

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

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.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Wet hands thoroughly with product and allow to dry without wiping.
  • For children under 6, use only under adult supervision.
  • Not recommended for infants.

OTHER SAFETY INFORMATION

Other Information

  • Do not store above 105º.
  • May discolor some fabrics.
  • Harmful to wood finishes and plastics.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Aloe, Potassium Sorbate, Xanthan Gum, Citric Acid Monohydrate, Ascorbic Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83169-100183169-1001-1

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
NameUNIIKind
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
CITRUS SINENSIS FRUIT OILWV48LBL15QIACT
XANTHAN GUMTTV12P4NEEIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
ISOPROPYL ALCOHOLND2M416302ACTIB
ALOEV5VD430YW9IACT

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
0e4a909a-d236-0685-e063-6294a90a0ea8efdd2ac8-9a98-9b81-e053-2a95a90aa46e2024-01-06WarningsExact identifier
spl set id: efdd2ac8-9a98-9b81-e053-2a95a90aa46e

Reported adverse events (FAERS/openFDA)#

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