Bahama Bos Hand Sanitizer

Manufacturer
Worthy Promotional Products, LLC
Effective date
2020-05-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:32:46

Label at a glance#

ProductBahama Bos Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

Helps decrease bacteria on the skin.

Dosage and administration

• Wet hands thoroughly with product. Briskly rub hands together until dry. Supervise children in the use of this product.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Hand Antiseptic

Uses

INDICATIONS & USAGE SECTION

Helps decrease bacteria on the skin.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • in the eyes. In case of contact, flush eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

  • if redness or irritation develop and persist for more than 72 hours.

Keepout 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 hands together until dry. Supervise children in the use of this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, carbomer, triethanolamine

Other Information

SPL UNCLASSIFIED SECTION

Store at 20° to 25°C (68° to 77°F) May discolor certain fabrics.

Package Labeling: 2 oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling: 4.2 oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling: 16.9 oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Package Labeling: 33.8 oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4Label4

Products#

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DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52260-00252260-002-60, 52260-002-12, 52260-002-50, 52260-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
eeddddf8-ef5f-f1eb-e053-2a95a90aaaaa3f3bf36b-ebec-4382-8178-bc0b99d8e3872022-12-02WarningsExact identifier
spl set id: 3f3bf36b-ebec-4382-8178-bc0b99d8e387

Reported adverse events (FAERS/openFDA)#

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