Purify instant Hand Sanitizer

Manufacturer
Purify Solutions Inc.
Effective date
2020-07-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:47

Label at a glance#

ProductPurify instant Hand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Indications and uses

Use as a hand sanitizer in the absence of soap and water, to reduce bacteria on the skin which may cause illness. Recommended for repeated use.

Dosage and administration

Spray hand sanitizer onto hands or enough to thoroughly cover hands. Rub hands together briskly for 30 seconds or until dry. Children under 6 years of age must be supervised when using the product

Storage and handling

Do not store above 110°F (43°C). May discolor certain fabrics or substances.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%, USP

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Use as a hand sanitizer in the absence of soap and water, to reduce bacteria on the skin which may cause illness.

Recommended for repeated use.

Warnings

WARNINGS SECTION

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

When Using This Product: 

  • Do not use in or near the eyes, or inhale.
  • In case of contact, rinse eyes thoroughly with water.

Stop use and contact your doctor if a rash or irritation appear and persist at the site of contact.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help immediately or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Spray hand sanitizer onto hands or enough to thoroughly cover hands. Rub hands together briskly for 30 seconds or until dry.
  • Children under 6 years of age must be supervised when using the product

Other information

STORAGE AND HANDLING SECTION

  • Do not store above 110°F (43°C). May discolor certain fabrics or substances.

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe (aloe barbadensis) juice, carbomer 940NF, dl-alpha-tocopheryl acetate, triethanolamine glycerin.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581698isopropyl alcohol 70 % Topical GelPSN1
581698isopropyl alcohol 0.7 ML/ML Topical GelSCD1
581698isopropyl alcohol 70 % Topical GelSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79660-001-01Purify instant Hand Sanitizer60 mL in 1 BOTTLE, SPRAYLIQUID601
79660-001-02Purify instant Hand Sanitizer60 mL in 1 BOTTLE, SPRAYLIQUID601
79660-001-02Purify instant Hand Sanitizer3 in 1 PACKAGELIQUID31
79660-001-03Purify instant Hand Sanitizer60 mL in 1 BOTTLE, SPRAYLIQUID601
79660-001-03Purify instant Hand Sanitizer6 in 1 PACKAGELIQUID61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79660-001PURIFY INSTANT HAND SANITIZER (ISOPROPYL ALCOHOL) LIQUID [PURIFY SOLUTIONS INC.]1Legacy NDC, 5 package rows20200718_3336e686-2ea8-4e61-ad8d-bde42aca2529.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79660-00179660-001-01, 79660-001-02, 79660-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
74700448-a94e-47b9-bb77-9d05a35cb6403336e686-2ea8-4e61-ad8d-bde42aca25292020-07-13WarningsExact identifier
spl id: 74700448-a94e-47b9-bb77-9d05a35cb640
spl set id: 3336e686-2ea8-4e61-ad8d-bde42aca2529

Reported adverse events (FAERS/openFDA)#

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