Hand Sanitizer Spray 5 oz

Manufacturer
Assured Bio Labs, LLC
Effective date
2020-10-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:09:27

Label at a glance#

ProductAssured Bio Infection Protection Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hands throughly with product and allow to dry without wiping.

Storage and handling

Do not store above 115°F

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 80% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only: hands Flammable. Keep away from heat or flame.

OTC - DO NOT USE SECTION

Do not use

  • on children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product

  • Do not use in eyes. In case of contact with eyes, rinse with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if redness and irritation develop and persist.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands throughly with product and allow to dry without wiping.

Other information

STORAGE AND HANDLING SECTION

  • Do not store above 115°F

Inactive ingredients

INACTIVE INGREDIENT SECTION

Fragrance, glycerin, isopropyl alcohol, purified water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

148 mL NDC: 79334-002-01 148 mL NDC: 79334-002-01148 mL NDC: 79334-002-01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79334-002-012022-09-27C16284748780-1c7ccaba7-14be-fd44-e053-dadaa90aa01bHand Sanitizer Spray 5 oz
79334-002-012021-07-23C16284748780-1c7ccaba7-14be-fd44-e053-dadaa90aa01bHand Sanitizer Spray 5 oz

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
79334-00279334-002-01

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
e8a86606-151e-30e0-e053-2a95a90a8beeb2c2718b-4763-f9f0-e053-2a95a90aaab42022-09-14WarningsExact identifier
spl set id: b2c2718b-4763-f9f0-e053-2a95a90aaab4

Reported adverse events (FAERS/openFDA)#

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