Azer Hand Sanitizer

Manufacturer
Azer Scientific, Inc.
Effective date
2020-04-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:06:44

Label at a glance#

ProductAzer Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommended for repeated use

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants Change from COVID template to match current labeling

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warning

WARNINGS SECTION

For external use only: hands

Flammable, keep away from fire or flame

When using this product, keep out of eyes. In case of contact with eyes, flush throughly with water. Avoid contact with broken skin. Do not inhale or ingest

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Irritation and redness develop
  • Condition persists for more than 72 hours

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Dosage and administration changes

RECENT MAJOR CHANGES SECTION

Change from COVID template to match current labeling

Other Information

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION


• Purified water • Glycerin • Carbomer • Triethanolamine • Aloe Vera Oil
• Aloe Vera gel • Tocopherol Acetate • Fragrance

Questions?

OTC - QUESTIONS SECTION

1-877-770-2937

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Azer Hand

Sanitizer Gel

Alcohol Antiseptic 62%

With Moisturizing

Aloe Vera & Citrus Scent

16 fl. oz. (473 mL) NDC: 74086-650-02

BOTTLE LABELBOTTLE LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN3
581660ethanol 0.62 ML/ML Topical GelSCD3
581660ethanol 62 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74086-650-032022-01-28C16284748780-1d6a99b39-a3d7-a426-e053-dadaa90af4c2Azer Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74086-650-03Azer Hand Sanitizer473 mL in 1 BOTTLE, DISPENSINGGEL4733

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74086-650AZER HAND SANITIZER (ALCOHOL) GEL [AZER SCIENTIFIC, INC.]3Legacy NDC, 1 package rows20200418_a32fd75f-a6a7-4826-e053-2995a90a64b4.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74086-65074086-650-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
a37bd4b5-9ff3-99ed-e053-2995a90a4e51a32fd75f-a6a7-4826-e053-2995a90a64b42020-04-17WarningsExact identifier
spl id: a37bd4b5-9ff3-99ed-e053-2995a90a4e51
spl set id: a32fd75f-a6a7-4826-e053-2995a90a64b4

Reported adverse events (FAERS/openFDA)#

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