FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
INBC TRADING, LLC
Effective date
2020-04-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:34:51

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

Flammable. Keep away from fire & flame. For external use hands only

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ irritation or redness develops ■ conditions persist for more than 72 hours ■ redness is present

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, contact a doctor or Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

SPL UNCLASSIFIED SECTION

■ Do not store above105ºF ■ May discolor some fabrics ■ Harmful to wood finishes and plastics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

carbomer, glycerin, triethanolamine, water

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74673-001-082025-11-13C16284748780-1d6a99b39-3b42-a426-e053-dadaa90af4c2Herbacil Hand Sanitizer
74673-001-162025-11-13C16284748780-1d6a99b39-3b42-a426-e053-dadaa90af4c2Herbacil Hand Sanitizer
74673-001-332025-11-13C16284748780-1d6a99b39-3b42-a426-e053-dadaa90af4c2Herbacil Hand Sanitizer
74673-001-422025-11-13C16284748780-1d6a99b39-3b42-a426-e053-dadaa90af4c2Herbacil Hand Sanitizer
74673-001-082022-01-28C16284748780-1d6a99b39-3b42-a426-e053-dadaa90af4c2Herbacil Hand Sanitizer
74673-001-162022-01-28C16284748780-1d6a99b39-3b42-a426-e053-dadaa90af4c2Herbacil Hand Sanitizer
74673-001-332022-01-28C16284748780-1d6a99b39-3b42-a426-e053-dadaa90af4c2Herbacil Hand Sanitizer
74673-001-422022-01-28C16284748780-1d6a99b39-3b42-a426-e053-dadaa90af4c2Herbacil Hand Sanitizer

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74673-001HAND SANITIZER (ALCOHOL) GEL [INBC TRADING, LLC]2Legacy NDC20200421_a2cb40a0-4e82-3fa9-e053-2995a90a4989.zip

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
74673-00174673-001-42, 74673-001-08, 74673-001-16, 74673-001-33

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
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT

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
424d5f90-4b84-361b-e063-6394a90a3f2aa2cb40a0-4e82-3fa9-e053-2995a90a49892025-11-05WarningsExact identifier
spl set id: a2cb40a0-4e82-3fa9-e053-2995a90a4989

Reported adverse events (FAERS/openFDA)#

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