Active Ingredient
BENZALKONIUM CHLORIDE 0.13%
Hill Country Essentials
FDA Label NDC 37808-721
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by H E B for the product Hill Country Essentials (NDC 37808-721). 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, when using this product, stop use and ask a doctor if, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
ANTIBACTERIAL
Uses
HELPS ELIMINATE BACTERIA ON HANDS
Warnings
FOR EXTERNAL USE ONLY
When Using This Product
AVOID CONTACT WITH EYES. IN CASE OF CONTACT, FLUSH WITH WATER
Stop Use And Ask A Doctor If
IRRITATION AND REDNESS DEVELOPS AND LASTS
Keep Out Of Reach Of Children
IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY
Directions
APPLY ONTO WET HANDS. LATHER AND RINSE THOROUGHLY
Other Information
STORE AT ROOM TEMPERATURE
Inactive Ingredients
WATER (AQUA), CETRIMONIUM CHLORIDE, GLYCERIN, LAURAMIDOPROPYLAMINE OXIDE, COCAMIDE MEA, SODIUM CHLORIDE, PEG-120 METHYL GLUCOSE DIOLEATE, FRAGRANCE (PARFUM), CITRIC ACID, TETRASODIUM EDTA, SODIUM SULFATE, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, RED 40 (CI 16035), YELLOW 5 (CI 19140), RED 33 (CI 17200)
Questions Or Comments?
1-866-695-3030
Label Copy
Image Of The Label (18270l)
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