FDA.reportPublic FDA data

ANTISEPTIC HAND SANITIZER

Manufacturer
Plaine Products
Effective date
2021-11-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:29:29

Label at a glance#

ProductANTISEPTIC HAND SANITIZER
Active ingredientALCOHOL
Label structure10 sections

Storage and handling

Other information  • store in a dry, cool place

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses  • hand sanitizer to decrease bacteria on the skin           

          •  recommended for repeated use

WARNINGS SECTION

Warnings

Flammable, keep away from fire/flame

For external use only

When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water

Stop use and ask a doctor if • irritation and redness develop • condition persists for 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 • wet hands thoroughly with product and allow to dry without wiping  • supervise children under 6 and not recommended for infants

STORAGE AND HANDLING SECTION

Other information  • store in a dry, cool place

INACTIVE INGREDIENT SECTION

Inactive ingredients  fragrance, water

OTC - QUESTIONS SECTION

Questions? +1-513-248-2017

You may also report serious side effects to this phone number. Mon - Fri 9:00 AM - 5:00 PM

SPL UNCLASSIFIED SECTION

peppermint fragrance

No Synthetic Fragrance, Vegan, Toxin Free, Cruelty Free, Triclosan Free

This bottle can be refilled with our full sized bottles. 

To order visit: WWW.PLAINEPRODUCTS.COM

Made in the USA

Manufactured for Plaine Products, Cincinnati, OH 45174 

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

untitleduntitled

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73757-41273757-412-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
fbcfd507-7bff-4a48-912e-aa786e62f3d75f4d2de9-a524-4d43-b02b-046c03809bc92023-09-07WarningsExact identifier
spl set id: 5f4d2de9-a524-4d43-b02b-046c03809bc9

Reported adverse events (FAERS/openFDA)#

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