Active Ingredient
ACTIVE INGREDIENTS:ETHYL ALCOHOL 62%
Dr Bronners
FDA Label NDC 73333-161
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nutrix International, Llc. for the product Dr Bronners (NDC 73333-161). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, indications & usage, warnings, inactive ingredient, keep out of reach of children, do not use, stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
ANTISEPTIC
Indications & Usage
USES: FOR HAND WASHING TO DECREASE BACTERIA ON SKIN.
Warnings
FOR EXTERNAL USE ONLY. FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.
Inactive Ingredient
WATER, GLYCERIN, LAVENDER OIL
Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.
Do Not Use
DO NOT USE IN THE EYES. IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER.
Stop Use
STOP USE AND ASK A DOCTOR IF IRRITATION AND REDNESS DEVELOP AND PERSIST FOR MORE THAN 72 HRS.
Dosage & Administration
SPRAY ON PALM, RUB HANDS TOGETHER. SUPERVISE CHILDREN.
Questions
QUESTIONS? CALL 760-743-2211
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Front Label (Label)
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