FDA.reportPublic FDA data

HEB Citrus Scented Hand Sanitizer Spray

Manufacturer
H.E.B.
Effective date
2024-10-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:25:54

Label at a glance#

ProductHEB Citrus Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Indications and uses

hand sanitizer to help reduce bacteria on the skin that could cause disease.

Dosage and administration

spray enough product in palm to thoroughly cover your hands rub hands together briskly until dry children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to help reduce bacteria on the skin that could cause disease.

Warnings

WARNINGS SECTION

For External use only

FLAMMABLE:

WARNINGS AND PRECAUTIONS SECTION

Keep away from heat or flame. Do not use while smoking.

Do not use

OTC - DO NOT USE SECTION

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

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes, ears and mouth. In case of contact with eyes, rinse thoroughly with water to remove.
  • do not puncture or incinerate. Contents under pressure. Do not store at temperuatres above 120º F.

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

Rash or irritation occurs. These may be signs of a serious condition.

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

  • spray enough product in palm to thoroughly cover your hands
  • rub hands together briskly until dry
  • children under 6 years of age should be supervised when using this product.

Other information

OTHER SAFETY INFORMATION

  • may discolor or damage some fabrics/ materials or surfaces.
  • avoid freezing and excessive heat above 40ºC (104ºF).

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, aloe barbadensis leaf juice, tocopheryl acetate, fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HEB54101D1HEB54101D1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1041849ethanol 70 % Topical SprayPSN2
1041849ethanol 0.7 ML/ML Topical SpraySCD2
1041849ethanol 70 % Topical SpraySY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37808-334-37HEB Citrus Hand Sanitizer156 g in 1 CANAEROSOL, SPRAY1562

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37808-334HEB CITRUS HAND SANITIZER (ALCOHOL) AEROSOL, SPRAY [H.E.B.]2Current NDC, Legacy NDC, 1 package rows20241017_c8ab20e5-6a20-5a6b-e053-2a95a90a247c.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
37808-33437808-334-37

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
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
HEB Citrus Hand SanitizerALCOHOLH.E.B.c8ab20e5-6a20-5a6b-e053-2a95a90a247c2024-10-15WarningsExact identifier
ndc (package): 37808-334-37
ndc (product): 37808-334
ndc11 (package): 37808033437
spl id: 2489b22e-7d02-8fdb-e063-6394a90acdb4
spl set id: c8ab20e5-6a20-5a6b-e053-2a95a90a247c

Reported adverse events (FAERS/openFDA)#

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