Hand Sanitizer Gel

Manufacturer
LS Promotions Inc.
Effective date
2025-04-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:59:14

Label at a glance#

ProductHand Sanitizer Gel
Active ingredientALCOHOL
Label structure13 sections

Indications and uses

To help decrease bacteria on hands.

Dosage and administration

Place enough product in your palm to thoroughly cover hand. Rub hands together briskly until dry. For children under 6 years old, use adult supervision.

Label contents#

Full prescribing information#

Drug Facts

DESCRIPTION SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • To help decrease bacteria on hands.

Warnings

WARNINGS SECTION

  • For external use only
  • Flammable, keep away from fire or flame

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes
  • In case of contact with eyes, flush thoroughly with water and then seek medical advise

Stop use and ask a doctor

OTC - STOP USE SECTION

  • If irritation or redness develops

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 immediately

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product in your palm to thoroughly cover hand.
  • Rub hands together briskly until dry.
  • For children under 6 years old, use adult supervision.

Other information

OTHER SAFETY INFORMATION

  • Do not store above 100°F

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients: water, triethanolamine, carbomer, propylene glycol, fragrance, tocopherol acetate, aloe vera oil.

Questions or Comments?

OTC - QUESTIONS SECTION

Call weekdays from 9 AM to 5 PM EST at 631-231-2300

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ABL1211 Hand Sanitizer Gel LabelABL1211 Hand Sanitizer Gel LabelABL1211 Hand Sanitizer Gel 16 NDC 72449-103-02

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72449-103-01Hand Sanitizer Gel2.9 mL in 1 PACKETGEL2.91
72449-103-02Hand Sanitizer Gel473 mL in 1 BOTTLE, PUMPGEL4731
72449-103-03Hand Sanitizer Gel50 mL in 1 BOTTLE, PLASTICGEL501
72449-103-04Hand Sanitizer Gel118 mL in 1 BOTTLE, PLASTICGEL1181
72449-103-05Hand Sanitizer Gel59 mL in 1 BOTTLE, PLASTICGEL591
72449-103-06Hand Sanitizer Gel236 mL in 1 BOTTLE, PLASTICGEL2361
72449-103-07Hand Sanitizer Gel295 mL in 1 BOTTLE, PUMPGEL2951
72449-103-08Hand Sanitizer Gel236 mL in 1 BOTTLE, PUMPGEL2361
72449-103-09Hand Sanitizer Gel473 mL in 1 BOTTLE, PLASTICGEL4731
72449-103-10Hand Sanitizer Gel29 mL in 1 BOTTLE, PLASTICGEL291
72449-103-11Hand Sanitizer Gel295 mL in 1 BOTTLE, PLASTICGEL2951

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72449-103HAND SANITIZER GEL GEL [LS PROMOTIONS INC.]1Current NDC, 11 package rows20250417_32d72358-9273-617c-e063-6294a90a6821.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
Hand Sanitizer GelHAND SANITIZER GELLS Promotions Inc.32d72358-9273-617c-e063-6294a90a68212025-04-14WarningsExact identifier
ndc (package): 72449-103-06
ndc (package): 72449-103-09
ndc (package): 72449-103-07
ndc (package): 72449-103-05
ndc (package): 72449-103-04
ndc (package): 72449-103-01
ndc (package): 72449-103-03
ndc (package): 72449-103-11
ndc (package): 72449-103-02
ndc (package): 72449-103-10
ndc (package): 72449-103-08
ndc (product): 72449-103
ndc11 (package): 72449010306
ndc11 (package): 72449010307
ndc11 (package): 72449010301
ndc11 (package): 72449010309
ndc11 (package): 72449010308
ndc11 (package): 72449010310
ndc11 (package): 72449010305
ndc11 (package): 72449010304
ndc11 (package): 72449010302
ndc11 (package): 72449010311
ndc11 (package): 72449010303
spl id: 32363324-b29e-68f6-e063-6294a90a5f59
spl set id: 32d72358-9273-617c-e063-6294a90a6821

Reported adverse events (FAERS/openFDA)#

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