FDA.reportPublic FDA data

hand sanitizer spray

Manufacturer
Broder Bros Co.
Effective date
2021-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:51:19

Label at a glance#

ProductAntibacterial Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

For hand sanitizing

Dosage and administration

Wet hands thoroughly with product, briskly rub together until dry Always supervise children in the use of this product Children under the age of 6 months: ask a doctor

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing

Warnings

WARNINGS SECTION

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

OTC - STOP USE SECTION

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

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product, briskly rub together until dry

Always supervise children in the use of this product

Children under the age of 6 months: ask a doctor

Other information

SPL UNCLASSIFIED SECTION

Store at 66° to 77° F (22° to 25° C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbomer, fragrance, glycerin, propylene glycol, tocopheryl acetate, triethanolamine, water

Questions?

OTC - QUESTIONS SECTION

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

SPL UNCLASSIFIED SECTION

Distributed By

Broder Bros Co., dba Prime Line

Gaffney, SC 29341

Made in China

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71513-20171513-201-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT

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
0e861601-a049-6f05-e063-6394a90a75bbbae9a0b7-d205-e194-e053-2995a90aae742024-01-01WarningsExact identifier
spl set id: bae9a0b7-d205-e194-e053-2995a90aae74

Reported adverse events (FAERS/openFDA)#

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