Cavalry

Manufacturer
CAVALRY SANITIZERS, L.L.C.
Effective date
2020-08-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:23:57

Label at a glance#

ProductCavalry
Active ingredientALCOHOL
Label structure12 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#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 72% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

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

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash occurs. These may be signs of a serious condition.

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

  • 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

ethyl acrylate copolymer*, ethyl methacrylate*, fragrance (parfum), glycerin, purified water USP, triethanolamine

* Contains one or more of these ingredients

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 75460-072-38

CAVALRYTM

SANITIZING SOLUTION

Alcohol Antiseptic 72% Topical Gel

Hand Sanitizer

Non-Sterile Gel

1 Gallon (3.78 L)

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1052530ethanol 72 % Topical SolutionPSN2
1052530ethanol 0.72 ML/ML Topical SolutionSCD2
1052530ethanol 72 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75460-072-382022-01-28C16284748780-1d6a99b39-921f-a426-e053-dadaa90af4c2da6807dd-c7d7-4e07-94d8-b36c99c80ffd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75460-072-38Cavalry3.78 L in 1 CANSOLUTION3.782

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75460-072CAVALRY (ALCOHOL) SOLUTION [CAVALRY SANITIZERS, L.L.C.]2Legacy NDC, 1 package rows20200806_da6807dd-c7d7-4e07-94d8-b36c99c80ffd.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75460-07275460-072-38

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
ffddb603-2bb5-4df3-9201-bb4d319394c3da6807dd-c7d7-4e07-94d8-b36c99c80ffd2020-08-05WarningsExact identifier
spl id: ffddb603-2bb5-4df3-9201-bb4d319394c3
spl set id: da6807dd-c7d7-4e07-94d8-b36c99c80ffd

Reported adverse events (FAERS/openFDA)#

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