Prevent Foam Sanitizer

Manufacturer
Eco-Med Pharmaceuticals, Inc.
Effective date
2020-08-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:24:18

Label at a glance#

ProductPrevent Foam Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Indications and uses

For personal hand hygiene to help prevent the spread of bacteria. For occasional use.

Dosage and administration

- Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • For personal hand hygiene to help prevent the spread of bacteria. For occasional use.

Warnings.

WARNINGS SECTION

Flammable. Keep away from open flame and sources of heat

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Supervise children when they use this product.

SPL UNCLASSIFIED SECTION

For external use only. If accidental ingestion occurs, call a Poison Control Center immediately.

Avoid contact with the eyes. If contact occurs, flush eyes with water. If irritation develops, discontinue use and consult a health care practitioner.

Directions

DOSAGE & ADMINISTRATION SECTION

- Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Cocamidopropyl betaine, Bis-PEG-12 Dimethicone, Glyceryl Caprylate, Dimethyl Lauramide, Glycerin, Aloe Barbadensis Leaf Powder, DL-alpha Tocopheryl Acetate (Vitamin E)

For domestic/personal care use.

SPL UNCLASSIFIED SECTION

Store below 43° C (110° F).

May discolour certain fabrics.

Questions :

OTC - QUESTIONS SECTION

1-844-432-6633 Mon -Fri 8am - 4pm (EST)

Email: info@eco-med.com

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:78835-002-37

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label6Label6

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2387551isopropyl alcohol 75 % Topical FoamPSN2
2387551isopropyl alcohol 0.75 ML/ML Topical FoamSCD2
2387551isopropyl alcohol 75 % Topical FoamSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78835-002-162022-01-28C16284748780-1d6a99b39-f9ac-a426-e053-dadaa90af4c2Prevent+ Foam Sanitizer
78835-002-372022-01-28C16284748780-1d6a99b39-f9ac-a426-e053-dadaa90af4c2Prevent+ Foam Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78835-002-16Prevent Foam Sanitizer500 mL in 1 BOTTLELIQUID5002
78835-002-37Prevent Foam Sanitizer3785 mL in 1 JUGLIQUID37852

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78835-002PREVENT FOAM SANITIZER (ISOPROPYL ALCOHOL) LIQUID [ECO-MED PHARMACEUTICALS, INC.]2Legacy NDC, 2 package rows20200811_ac2348e1-4937-3f92-e053-2995a90a0d73.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78835-00278835-002-16, 78835-002-37

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
ac8b9268-a058-4033-e053-2995a90a5655ac2348e1-4937-3f92-e053-2995a90a0d732020-08-10WarningsExact identifier
spl id: ac8b9268-a058-4033-e053-2995a90a5655
spl set id: ac2348e1-4937-3f92-e053-2995a90a0d73

Reported adverse events (FAERS/openFDA)#

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