FDA.reportPublic FDA data

Amcon Labs Hand Sanitizer Fragrance Free Gel Sanitizer

Manufacturer
Nomax, Inc.
Effective date
2026-09-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-09-26 01:01:46

Label at a glance#

ProductAmcon Labs Hand Sanitizer Fragrance Free Gel Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Place a small amount of product in one hand. Spread on hands and run into skin until dry. Place a smaller amount into one hand and spread over both hands and wrists. Rub into skin until dry. Children should be supervised while using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 60% v/v

Purpose

OTC - PURPOSE SECTION

Skin Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce amount of bacteria on the skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only. If swallowed, seek medical attention.

When using this product do not use around or near the eyes. If contact occurs, flush eyes with water and contact doctor immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place a small amount of product in one hand.
  • Spread on hands and run into skin until dry.
  • Place a smaller amount into one hand and spread over both hands and wrists.
  • Rub into skin until dry.
  • Children should be supervised while using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Carbomer, Glycerin, Triethanolamine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Label - 8 fl. oz. Bottle with PumpProduct Label - 8 fl. oz. Bottle with Pump

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51801-43751801-437-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22023-11-20full-release2026-06-01 00:02:28

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
0a985160-e7c4-ee16-e063-6294a90ae08a0219f330-81c0-c67f-e063-6394a90a4da92023-11-20WarningsExact identifier
spl set id: 0219f330-81c0-c67f-e063-6394a90a4da9

Reported adverse events (FAERS/openFDA)#

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