Active Ingredient
BENZETHONIUM CHLORIDE 0.1 PERCENT
Antimicrobial Foaming
FDA Label NDC 63148-241
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Apollo Health And Beauty Care for the product Antimicrobial Foaming (NDC 63148-241). 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, keep out of reach of children, when using this product, stop using this product and ask a doctor, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
ANTIMICROBIAL
Uses
FOR WASHING TO DECREASE BACTERIA ON THE SKIN.
Warnings
FOR EXTERNAL USE ONLY.
Keep Out Of Reach Of Children
IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.
When Using This Product
AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER.
Stop Using This Product And Ask A Doctor
IF IRRITATION OR REDNESS DEVELOPS AND LASTS.
Directions
PUMP INTO WET HANDS. WORK INTO A LATHER VIGOROUSLY. RINSE THOROUGHLY.
Inactive Ingredients
WATER, COCAMIDOPROPYL BETAINE, GLYCERIN, DECYL GLUCOSIDE, POLYQUATERNIUM-7, FRAGRANCE, CAMELLIA SINENSIS, ZINGIBER OFFICINALE, HIBISCUS SABDARIFFA, CHAMOMILA RECUTITA, CITRIC ACID, ORIGANUM VULGARE LEAF EXTRACT, THYMUS VULGARE (THYME) EXTRACT, CINNAMOMUM ZEYLANICUM BARK EXTRACT, ROSEMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT, LAVANDULA ANGUSTIFOLIA (LAVENDER) FLOWER EXTRACT, HYDRASTIS CANADENSIS (GOLDEN SEAL) ROOT EXTRACT, TETRASODIUM EDTA, GREEN 5, RED 33, YELLOW 5.
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