CLOROX Hand sanitizer Gel

Manufacturer
New Wave Global Services Inc
Effective date
2023-12-27
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:16:46

Label at a glance#

ProductCLOROX Hand sanitizer Gel
Active ingredientALCOHOL
Label structure14 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Acrylates/Vinyl Isodecanoate Crosspolymer (10000 MPA.S Neutralized at 0.5%), Aloe Vera Leaf Extract, Propylene Glycol, Isopropyl Myristate, Fragrance, Vitamin E Acetate, Yellow 10, Yellow 5, Blue 1

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CLOROX Hand Sanitizer Gel 12 Oz Bottle-NDC: 80714-034-10CLOROX Hand Sanitizer Gel 12 Oz Bottle-NDC: 80714-034-10

Clorox Hand Sanitizer Gel 8 Oz Bottle-NDC: 80714-034-09Clorox Hand Sanitizer Gel 8 Oz Bottle-NDC: 80714-034-09

clorox HS 4OZx12 Carton, NDC:80714-034-04

CLOROX HS 4OZX12 CARTONCLOROX HS 4OZX12 CARTON

CLOROX HS 4OZ Tube, NDC: 80714-034-02

Clorox HS 4OZ TubeClorox HS 4OZ Tube

CLOROX HS Gallon Jug- NDC 80714-034-08

CLOROX HS Gallon JugCLOROX HS Gallon Jug

CLOROX HS Pouch-NDC 80714-034-05 Clorox HS Pouch- NDC 80714-034-05Clorox HS Pouch- NDC 80714-034-05

CLOROX HS 24x Single Use Pouches Carton- NDC 80714-034-06 24x Single Use Pouces Carton NDC 80714-034-0624x Single Use Pouces Carton NDC 80714-034-06

CLOROX HS 12X2oz Tube Display Carton- NDC 80714-034-03 12x2 oz Tubes Display Carton12x2 oz Tubes Display Carton

CLOROX HS 2OZ Tube-NDC 80714-034-01

Clorox Hand Sanitizer Gel - 2oz Tube Label NDC: 80714-034-01Clorox Hand Sanitizer Gel - 2oz Tube Label NDC: 80714-034-01

6 x 12 oz Bottles

6 x 12 oz Bottles6 x 12 oz Bottles

Products#

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NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

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
0d8507ac-785d-f790-e063-6294a90a2991b2e9ab98-d2a6-257b-e053-2a95a90a08f52023-12-27WarningsExact identifier
spl id: 0d8507ac-785d-f790-e063-6294a90a2991
spl set id: b2e9ab98-d2a6-257b-e053-2a95a90a08f5

Reported adverse events (FAERS/openFDA)#

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