FDA.reportPublic FDA data

biom Sanitizing Alcohol Wipes - Eucalyptus Chill

Manufacturer
Biom Innovations Inc
Effective date
2024-12-24
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:48:32

Label at a glance#

Productbiom Sanitizing Alcohol Wipes - Eucalyptus Chill
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Wipe hands thoroughly. Discard after use. Ethanol 65%. Wipe hands thoroughly. Discard after use.

Storage and handling

Store below 104° F (40° C). Each wipe is 15 x 20 cm. May discolor certain fabrics. Do not use as a baby wipe, on the face, or in the genital area.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

This hand sanitizer (65%(w/w) ethanol in an aqueous solution):

- Is manufactured using United States Pharmacopoeia (USP) grade ingredients.

- The alcohol (ethanol) is (USP or Food Chemical Codex (FCC) grade), and is denatured according to Alcohol & Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 65% w/w. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Reducing bacteria on skin.

Directions

INDICATIONS & USAGE SECTION

Wipe hands thoroughly. Discard after use.

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Ethanol 65%. Wipe hands thoroughly. Discard after use.

Warnings

WARNINGS SECTION

Flammable. Keep away from Fire and Flame. External Use Only. Do not use in eyes. If contact occurs, flush thoroughly with water. Stop use and ask doctor if redness or irritation develops and continues for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact the poison control center immediately.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact the poison control center immediately.

Other information

STORAGE AND HANDLING SECTION

Store below 104° F (40° C).
Each wipe is 15 x 20 cm.
May discolor certain fabrics.
Do not use as a baby wipe, on
the face, or in the genital area.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Eucalyptus Globulus Leaf Oil (Eucalyptus Essential Oil), Aloe Barbadensis Leaf Juice (Organic Aloe), Glycerin (Moisturizer)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10 wipes; NDC82311-0101-2

2023+ packet; 10 wipes.2023+ packet; 10 wipes.10 wipes; NDC82311-0101-210 wipes; NDC82311-0101-2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82311-0101-2biom Sanitizing Alcohol Wipes - Eucalyptus Chill42 mL in 1 PACKAGESWAB425

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82311-0101BIOM SANITIZING ALCOHOL WIPES - EUCALYPTUS CHILL (ALCOHOL) SWAB [BIOM INNOVATIONS INC]5Current NDC, Legacy NDC, 1 package rows20241225_d911fa72-3dc1-2d86-e053-2995a90aeb9c.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82311-010182311-0101-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
EUCALYPTUS GLOBULUS LEAFS546YLW6E6IACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
biom Sanitizing Alcohol Wipes - Eucalyptus ChillALCOHOLBiom Innovations Inc23a89b5b-ee5f-4480-e063-6394a90a03b42026-09-02WarningsExact identifier
ndc (product): 82311-0101
2a02b644-1c29-26de-e063-6294a90adeb8d911fa72-3dc1-2d86-e053-2995a90aeb9c2024-12-24WarningsExact identifier
spl id: 2a02b644-1c29-26de-e063-6294a90adeb8
spl set id: d911fa72-3dc1-2d86-e053-2995a90aeb9c

Reported adverse events (FAERS/openFDA)#

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