bt Hand Sanitizer

Manufacturer
PLZ Corp
Effective date
2023-01-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:39:53

Label at a glance#

Productbt Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Storage and handling

Other information Store between 59-86°F (15-30°C) Avoid freezing and excessive heat above 104°F (40“C)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Alcohol 70% v/v

OTC - PURPOSE SECTION

Purpose
Antiseptic

INDICATIONS & USAGE SECTION

Use

to help reduce bacteria on skin that can potentially cause disease

WARNINGS SECTION

Warnings
For external use only.
Flammable. Keep away from heat or flame.

OTC - WHEN USING SECTION

When using this product keep away from eyes. In case of eye contact, rinse eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • apply liberally to hands to cover all surfaces
  • rub hands together until dry
  • supervise children under 6 years old
  • not recommended for infants

STORAGE AND HANDLING SECTION

Other information

  • Store between 59-86°F (15-30°C)
  • Avoid freezing and excessive heat above 104°F (40“C)

INACTIVE INGREDIENT SECTION

Inactive ingredients

Carbomer, isopropyl myristate, triethanolamine, vegetable glycerin, water

SPL UNCLASSIFIED SECTION

Made in Canada with globally sourced materials

Distributed by:

K-G Spray-Pak, Inc. (Assured Packaging Division)

2651 Warrenville Rd. Ste 300

Downers Grove, IL 60515

Questions?

866-836-8855; www.kgpackaging.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

bt™

HAND SANITIZER

ALCOHOL 70% TOPICAL SOLUTION

Antiseptic Hand Rub

Non-Sterile Solution

3.4 Fl Oz (100 mL)

labellabel

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64591-100064591-1000-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML · Source PDF

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
0687a8a5-d329-acab-e063-6294a90a1018a45e9d88-b54c-bac2-e053-2a95a90ad42f2023-09-29WarningsExact identifier
spl set id: a45e9d88-b54c-bac2-e053-2a95a90ad42f

Reported adverse events (FAERS/openFDA)#

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