Bare Hands

Manufacturer
Coola, LLC | EC Labs | Natures Formulae Health Products Ltd.
Effective date
2020-09-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:15:39

Label at a glance#

ProductBare Hands
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

- to help reduce bacteria on skin. - for repeated use.

Dosage and administration

· Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry. · Recommended for repeated use.

Storage and handling

· Do not store abot 104F (40C) · May discolor some fabrics · Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Ethyl Alcohol 70%.........Antiseptic

Uses

INDICATIONS & USAGE SECTION

- to help reduce bacteria on skin. - for repeated use.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire/flame.

For external use only.

OTC - WHEN USING SECTION

Whe using this product: avoid contact with eyes. · in case of eye contact, immediately flush eyes with water, call a doctor. · Avoid contact with broken skin.

OTC - STOP USE SECTION

Discontinue use if irritation or redness develops. If condition persists for than 72 hours, consult a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Children should only use this product under adult supervision. Do not drink. Not edible. In case of accidental ingestion seek professional assistance or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

· Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry. · Recommended for repeated use.

Other Information

STORAGE AND HANDLING SECTION

· Do not store abot 104F (40C) · May discolor some fabrics · Harmful to wood finishes and plastics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Allyl Heptoate, Benzyl Alcohol, Caprylic/Capric Triglyceride, Carthamus Tinctorius (Safflower) Oleosomes, Gamma-Decalactone, Gamme-Nonalactone, Gamme-Octalactone, Glycerin, Heliotopine, Polyacrylate Crosspolymer-6, Raspberry Ketone, Sodium Hydroxide, Triethyl Citrate, Vanillin, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

Products#

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DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79753-00179753-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
f0ff41cc-42d7-ed95-e053-2a95a90a7828ae82f3c5-d295-4f20-e053-2a95a90a0f1e2022-12-29WarningsExact identifier
spl set id: ae82f3c5-d295-4f20-e053-2a95a90a0f1e

Reported adverse events (FAERS/openFDA)#

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