FDA.reportPublic FDA data

Clorox Hand Sanitizer

Manufacturer
Brand Buzz LLC
Effective date
2025-03-03
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:56:53

Label at a glance#

ProductClorox Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

Hand sanitizing to help reduce bacteria on the skin.

Dosage and administration

Wet hands thoroughly with product and allow to dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizing to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
  • Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a physician.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Disodium Cocoamphodiacetate, Phenoxyethanol, Aloe, Barbadensis Leaf Juice, Chamomile Flower Extract, Sodium Benzoate, Potassium Sorbate, Quaternium-52, PEG-75 Lanolin, PEG-8 Dimethicone, Dosodium EDTA, Citric Acid, Cetylpyridium Chloride

Questions of Comments?

OTC - QUESTIONS SECTION

Visit us at www.brandbuzzcp.com or call us at 1-888-508-4750

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CLOROX PRO™

CLOROX™

Hand Sanitizing Wipes

Kills 99.99% Germs*

  • Cleans hands
  • Bleach-Free

CloroxPro™ Hand Sanitizing Wipes kill 99.99% of mopst illness causing germs, so you can clean your hands with confidence.

*kills 99.99% of most illness causing germs

Wipe dimensions: 5.75in. x 7.5in. (14.6 cm x 19 cm)

  1. Remove lid by lifting upward.
  2. Pull wipe from center of the roll and thread through the underside of lid. DO NOT put finger through the hole.
  3. Close lid and pull wipe from canister at an angle.
  4. Snap lid cap shut to retain moisture.

To Dispose: Place in waste basket after use. DO NOT FLUSH

Developed in USA | Responsibly Made in China ©2021

Distributed by Brand Buzz LLC., 1407 Broadway, NEw York, NY 10018

CLOROX and other trademarks are used by Brand Buzz LLC under license from The Clorox Company or its affiliates.

20 WIPES

2020

40 WIPES

4040

100 WIPES

100100

270 WIPES

270270

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN5
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD5
1038558benzalkonium chloride 0.13 % Topical ClothSY5
1038558benzalkonium chloride 0.13 % Topical SwabSY5
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY5
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY5
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69540-0036-1Clorox Hand Sanitizer0.13 g in 1 PATCHCLOTH0.135
69540-0036-1Clorox Hand Sanitizer20 in 1 POUCHCLOTH205
69540-0036-2Clorox Hand Sanitizer40 in 1 CANISTERCLOTH405
69540-0036-2Clorox Hand Sanitizer0.13 g in 1 PATCHCLOTH0.135
69540-0036-3Clorox Hand Sanitizer100 in 1 CANISTERCLOTH1005
69540-0036-3Clorox Hand Sanitizer0.13 g in 1 PATCHCLOTH0.135
69540-0036-4Clorox Hand Sanitizer270 in 1 CANISTERCLOTH2705
69540-0036-4Clorox Hand Sanitizer0.13 g in 1 PATCHCLOTH0.135

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69540-0036CLOROX HAND SANITIZER (BENZALKONIUM CHLORIDE) CLOTH [BRAND BUZZ LLC]5Legacy NDC, 8 package rows20250309_e9611e76-c1df-4065-a965-c92d82b31f60.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69540-003669540-0036-1, 69540-0036-2, 69540-0036-3, 69540-0036-4

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
PEG-75 LANOLIN09179OX7TBIACT
QUATERNIUM-52588EQF3H1PIACT
PEG-8 DIMETHICONEGIA7T764ODIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
MATRICARIA CHAMOMILLA FLOWERING TOP3VNC7T6Z02IACT
PHENOXYETHANOLHIE492ZZ3TIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
CETYLPYRIDINIUM CHLORIDED9OM4SK49PIACT
SODIUM BENZOATEOJ245FE5EUIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2f6a3062-891d-971d-e063-6394a90a8536e9611e76-c1df-4065-a965-c92d82b31f602025-03-03WarningsExact identifier
spl id: 2f6a3062-891d-971d-e063-6394a90a8536
spl set id: e9611e76-c1df-4065-a965-c92d82b31f60

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.