Hand Sanitizer

Manufacturer
Broder Bros Co.
Effective date
2022-11-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:47:24

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire and flame.

For external use only

When using this product

OTC - WHEN USING SECTION

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

Stop use & ask doctor if

OTC - STOP USE SECTION

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 contact a Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

SPL UNCLASSIFIED SECTION

  • Store at 68°F to 77°F (20°C to 25°C).

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Carbopol 940, Fragrance, Triethanolamine, Water.

Questions?

OTC - QUESTIONS SECTION

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

SPL UNCLASSIFIED SECTION

Hand Sanitizer

Net. wt. 2.19 Fl. oz. (65mL)

Lot no: Use by:

Made in China

Dist. by: Broder Bros. Co., dba Prime Line

Bridgeport, CT 06610/Gaffney, SC 29341

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71513-10271513-102-01, 71513-102-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
TROLAMINE9O3K93S3TKIACT
CARBOMER 9404Q93RCW27EIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
09aba42f-d98f-32f8-e063-6294a90aead4d4b45a38-4e81-9dcb-e053-2a95a90aa5762024-01-01WarningsExact identifier
spl set id: d4b45a38-4e81-9dcb-e053-2a95a90aa576

Reported adverse events (FAERS/openFDA)#

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