FDA.reportPublic FDA data

Howe, Consulting

Manufacturer
Nutrix International, LLC.
Effective date
2020-05-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:10:16

Label at a glance#

ProductHowe, Consulting
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 age of 6 when using this product to avoid swallowing.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT(S)

OTC - ACTIVE INGREDIENT SECTION

​Alcohol 70% v/v.

PURPOSE

OTC - PURPOSE SECTION

FrontFrontAntiseptic

Use[s]

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

  • On children less than 2 months of age.
  • On open skin wounds.

When using

OTC - WHEN USING SECTION

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

Stop use

OTC - STOP USE SECTION

Stop use and ask doctor if 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

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

Other Information

OTHER SAFETY INFORMATION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Propylene Glycol, Glycerin, Methyl hydroxypropyl Cellulose

Drug Facts Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73333-016-012022-01-28C16284748780-1d6a99b39-bf83-a426-e053-dadaa90af4c2a5169f90-6503-06d6-e053-2995a90add5a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73333-016-01Howe, Consulting473 g in 1 BOTTLELIQUID4731

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73333-016HOWE, CONSULTING (PURTOUCH) LIQUID [NUTRIX INTERNATIONAL, LLC.]1Legacy NDC, 1 package rows20200508_a5169f90-6503-06d6-e053-2995a90add5a.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
73333-01673333-016-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYPROMELLOSES3NXW29V3WOIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT

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
a516a60c-472b-4bb8-e053-2995a90ac3b4a5169f90-6503-06d6-e053-2995a90add5a2020-05-07WarningsExact identifier
spl id: a516a60c-472b-4bb8-e053-2995a90ac3b4
spl set id: a5169f90-6503-06d6-e053-2995a90add5a

Reported adverse events (FAERS/openFDA)#

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