FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
J.R. Watkins, LLC.
Effective date
2020-11-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:07:12

Label at a glance#

ProductHand Sanitizer Unscented
Active ingredientAlcohol
Label structure10 sections

Indications and uses

To reduce bacteria on the skin Recommended for repeated use

Dosage and administration

Wet hands thoroughly and allow to dry without wiping. Children under 6, use adult supervision.

Storage and handling

Store below 110°F (43°C)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • To reduce bacteria on the skin
  • Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

Flammable: Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes, if contact occurs, rinse thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Irritation or redness develop
  • Condition persists 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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly and allow to dry without wiping.
  • Children under 6, use adult supervision.

Other information

STORAGE AND HANDLING SECTION

Store below 110°F (43°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Ethylhexylglycerin, Aloe Barbadensis Leaf Juice.

Questions?

OTC - QUESTIONS SECTION

Contact us at 1-888-384-1945

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ESTD
1868
J.R.
WATKINS
REMEDIES FOR BODY™

PLANT-BASED
HAND SANITIZER

MADE WITH ALOE EXTRACT

A naturally derived hand
sanitizer to cleanse hands and kill
germs while on-the-go.

UNSCENTED

4 FL OZ (118 mL)

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Label
PRINCIPAL DISPLAY PANEL - 118 mL Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72342-170-182024-02-13C16284748780-1f386c64a-429f-0266-e053-dadaa90a7c1aHand Sanitizer Unscented
72342-170-182023-01-30C16284748780-1f386c64a-429f-0266-e053-dadaa90a7c1aHand Sanitizer Unscented

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
72342-17072342-170-18

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
Alcohol3K9958V90MACTIB
Aloe Vera LeafZY81Z83H0XIACT
Ethylhexylglycerin147D247K3PIACT
GlycerinPDC6A3C0OXIACT
Water059QF0KO0RIACT

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
1131d1a3-2af8-ae55-e063-6394a90a18afac1326d7-bcff-4df7-b25b-2fe486e7fe292024-02-12WarningsExact identifier
spl set id: ac1326d7-bcff-4df7-b25b-2fe486e7fe29

Reported adverse events (FAERS/openFDA)#

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