Active Ingredient
ETHYL ALCOHOL (ORGANIC) 62%
Dr Bronners
FDA Label NDC 73333-160
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 73333-160). 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:, uses:, warnings:, do not use, inactive ingredients, keep out of reach of children, stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose:
ANTISEPTIC
Uses:
FOR HAND WASHING TO DECREASE BACTERIA ON SKIN.
Warnings:
FOR EXTERNAL USE ONLY. FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.
Do Not Use
DO NOT USE NEAR EYES. IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER.
DO NOT USE NEAR EYES. IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER.
Inactive Ingredients
WATER, ORGANIC GLYCERIN, ORGANIC PEPPERMINT 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.
Stop Use
STOP USE AND ASK A DOCTOR IF SKIN IRRITATION DEVELOPS.
Directions
SPRAY ON PALM, RUB HANDS TOGETHER. SUPERVISE CHILDREN UNDER 6.
Other Information
STORE AT 20° - 25°C (68° - 77°F)
Questions?
CALL 760-743-2211
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LABEL
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