ArroPure 70

Manufacturer
ARROPOL Chemicals, Inc.
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-05-31 23:46:45

Label at a glance#

ProductArroPure 70
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 15-30°C (59-86°F) Avoid freezing and excessive heat above 40°C (104°F)

Label contents#

Full prescribing information#

Active Ingredient[s]

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

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

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.

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

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

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

carbomer, fragrance, glycerin, trolamine, water

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label for all packages

for all packagesfor all packages

18,927 mL NDC: 77040-268-05

18927 ml label18927 ml label

208,198 mL NDC: 77040-268-55

208198 ml label208198 ml label

1,040,988 mL NDC: 77040-268-00

1040988 ml label1040988 ml label

3,785 mL NDC: 77040-268-01

3785 ml label3785 ml label1,000 mL NDC: 77040-268-11

1000 ml label1000 ml label500 mL NDC: 77040-268-16

500 ml label500 ml label237 mL NDC: 77040-268-08

237 ml label237 ml label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN8
581662ethanol 0.7 ML/ML Topical GelSCD8
581662ethanol 70 % Topical GelSY8
581662ethyl alcohol 70 % Topical GelSY8

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77040-268-00ArroPure 701040988 mL in 1 CONTAINERGEL10409888
77040-268-01ArroPure 703785 mL in 1 JUGGEL37858
77040-268-05ArroPure 7018927 mL in 1 PAILGEL189278
77040-268-08ArroPure 70237 mL in 1 BOTTLE, PLASTICGEL2378
77040-268-11ArroPure 701000 mL in 1 BOTTLE, PLASTICGEL10008
77040-268-16ArroPure 70500 mL in 1 BOTTLE, PLASTICGEL5008
77040-268-55ArroPure 70208198 mL in 1 DRUMGEL2081988

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77040-268ARROPURE 70 (ALCOHOL) GEL [ARROPOL CHEMICALS, INC.]8Legacy NDC, 7 package rows20220114_a49a6e30-05d5-993d-e053-2995a90a2684.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
77040-26877040-268-01, 77040-268-05, 77040-268-55, 77040-268-00, 77040-268-11, 77040-268-16, 77040-268-08

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 · Source PDF

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
d578be47-d15f-0481-e053-2995a90a565da49a6e30-05d5-993d-e053-2995a90a26842022-01-13WarningsExact identifier
spl id: d578be47-d15f-0481-e053-2995a90a565d
spl set id: a49a6e30-05d5-993d-e053-2995a90a2684

Reported adverse events (FAERS/openFDA)#

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