Dr Bronners

Manufacturer
Nutrix International, LLC.
Effective date
2022-05-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:49:32

Label at a glance#

ProductDr Bronners
Active ingredientALCOHOL
Label structure13 sections

Indications and uses

FOR HAND WASHING TO DECREASE BACTERIA ON SKIN.

Dosage and administration

SPRAY ON PALM, RUB HANDS TOGETHER. SUPERVISE CHILDREN UNDER 6.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL (ORGANIC) 62%

PURPOSE:

OTC - PURPOSE SECTION

ANTISEPTIC

USES:

INDICATIONS & USAGE SECTION

FOR HAND WASHING TO DECREASE BACTERIA ON SKIN.

WARNINGS:

WARNINGS SECTION

FOR EXTERNAL USE ONLY. FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.

DO NOT USE

OTC - DO NOT USE SECTION

DO NOT USE NEAR EYES. IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER, ORGANIC GLYCERIN, ORGANIC PEPPERMINT OIL

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 A POISON CONTROL CENTER RIGHT AWAY.

DO NOT USE

OTC - DO NOT USE SECTION

DO NOT USE NEAR EYES. IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER.

STOP USE

OTC - STOP USE SECTION

STOP USE AND ASK A DOCTOR IF SKIN IRRITATION DEVELOPS.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

SPRAY ON PALM, RUB HANDS TOGETHER. SUPERVISE CHILDREN UNDER 6.

OTHER INFORMATION

OTHER SAFETY INFORMATION

STORE AT 20° - 25°C (68° - 77°F)

QUESTIONS?

OTC - QUESTIONS SECTION

CALL 760-743-2211

DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front LabelFront LabelLABEL

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73333-160-01Dr Bronners59 g in 1 BOTTLELIQUID592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73333-160DR BRONNERS (HAND SANITIZER PEPPERMINT) LIQUID [NUTRIX INTERNATIONAL, LLC.]2Legacy NDC, 1 package rows20220511_acb2c20c-a768-9ec1-e053-2a95a90a36a1.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
73333-16073333-160-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
PEPPERMINT OILAV092KU4JHIACT
GLYCERINPDC6A3C0OXIACT
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
deb3ed11-8b79-7f96-e053-2995a90a5f76acb2c20c-a768-9ec1-e053-2a95a90a36a12022-05-10WarningsExact identifier
spl id: deb3ed11-8b79-7f96-e053-2995a90a5f76
spl set id: acb2c20c-a768-9ec1-e053-2a95a90a36a1

Reported adverse events (FAERS/openFDA)#

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