Clorox Antimicrobial
FDA Label NDC 69540-0029

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Brand Buzz Llc for the product Clorox Antimicrobial (NDC 69540-0029). 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, use, warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Use

  • For handwashing to decrease bacteria on skin

Warnings

For external use only.

In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water. If irritation persists, contact a Poison Control Center right away.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Directions

  • Apply onto wet hands, lather for 30 seconds and rinse thoroughly.

Inactive Ingredients

Water, Sodium Laureth Sulfate, Sodium Chlroride, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Laureth-3, Sodium Bicarbonate, Disodium EDTA, Fragrance, Methylchloroisothiazolinone, Blue 1 (Ci 42090), Blue S Nbl (Ci 61585).

Package Label.Principal Display Panel

Clorox

Antimicrobial

HandSoap

Ultra Concentrated Dishwashing Liquid

Fresh

with Oxi

Bleach-Free

22FL OZ

(1.375 PT) 650 mL

Label

Label (Fresh)

Label (Fresh)

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