FDA.reportPublic FDA data

hand sanitizer spray

Manufacturer
Broder Bros Co.
Effective date
2022-07-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:57:15

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Ethyl Alcohol 75%

OTC - PURPOSE SECTION

Purpose Antiseptic

INDICATIONS & USAGE SECTION

Use for hand sanitizing

WARNINGS SECTION

Warnings

  • Flammable. Keep away from heat and flame.
  • For external use only.

OTC - WHEN USING SECTION

When using this product

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

OTC - STOP USE SECTION

Stop use and ask a doctor

if irritation and redness develops and persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

if swallowed get medical help or call a Poison Control Center right away

DOSAGE & ADMINISTRATION SECTION

Directions

Wet hands thoroughly with product, briskly rub together until dry

Always supervise children in the use of this product

Children under 6 months of age: ask a doctor

SPL UNCLASSIFIED SECTION

Other information

Store at 68° to 77° F (22° to 25° C)

INACTIVE INGREDIENT SECTION

Inactive ingredients carbomer, glycerin, triethanolamine, water

OTC - QUESTIONS SECTION

Questions?

1-800-873-7746 M-F 8 am - 5 pm EST

SPL UNCLASSIFIED SECTION

Made in China

Distributed By: Broder Bros Co., dba Prime Line

Gaffney, SC 29341

Lot number:

Expiration date:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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
71513-10471513-104-07, 71513-104-01

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
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT

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
e34f3c81-6511-64ab-e053-2995a90a9bd8bccc9df0-76bb-3cdc-e053-2a95a90a65ce2022-07-08WarningsExact identifier
spl id: e34f3c81-6511-64ab-e053-2995a90a9bd8
spl set id: bccc9df0-76bb-3cdc-e053-2a95a90a65ce

Reported adverse events (FAERS/openFDA)#

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