Oars and Alps Antibacterial Hand Sanitizer Gel

Manufacturer
Oars and Alps LLC
Effective date
2022-11-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:48:37

Label at a glance#

ProductOars and Alps Antibacterial Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Helps reduce bacteria on the skin

Dosage and administration

Wet hands thoroughly with product and rub into skin until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Uses

INDICATIONS & USAGE SECTION

Helps reduce bacteria on the skin

Purpose

OTC - PURPOSE SECTION

Antibacterial

Warnings

WARNINGS SECTION

For external use only. Flammable, keep away from fire. Do not use on damaged or broken skin. Keep out of eyes. Rinse with water to remove. Stop use if rash occurs.If product is swallowed, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach with children.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and rub into skin until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Calendula Officinalis Flower Extract, Chamomilla Recutita (Matricaria) Flower Extract, Citric Acid, Glycerin, Hydroxypropyl Guar, Water

Questions or Comments

OTC - QUESTIONS SECTION

Contact (630)635-7839 or hi@oarsandalps.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83046-35983046-359-79

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
ed12a008-2a72-5839-e053-2a95a90ab39aed12a71d-e8f1-b336-e053-2a95a90a4f092022-11-09WarningsExact identifier
spl id: ed12a008-2a72-5839-e053-2a95a90ab39a
spl set id: ed12a71d-e8f1-b336-e053-2a95a90a4f09

Reported adverse events (FAERS/openFDA)#

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