Sanitizer Wipes

Manufacturer
Organic Filling Solutions, LLC
Effective date
2020-08-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:25:23

Label at a glance#

ProductSanitizer Wipes
Active ingredientALCOHOL
Label structure14 sections

Dosage and administration

Apply thoroughly to hands to cover all surfaces. Rub hands together until dry.

Storage and handling

Keep out of light, store at room temperature 59 - 86 degrees Farenheit

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

This is an alcohol wipe manufactured in the USA

  1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (75%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
  2. Glycerol (3.2% v/v)
  3. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Multi-purpose

Use

INDICATIONS & USAGE SECTION

Single use wipes for hands. Close properly after dispensing to maintain purity, as alcohol by nature evaporates quickly. Dispose properly. Apply thoroughly to hands to cover all surfaces. Rub hands together until dry.

Warnings

WARNINGS SECTION

For external use only, hands, general cleaning. Does not replace wipes for medical procedures. Flammable; keep away from fire or flame. Do not ingest.

Do not use

OTC - DO NOT USE SECTION

  • Stop use and ask a doctor if irritation and redness develop, condition persists for more than 72 hours
  • Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

OTC - WHEN USING SECTION

When using this product, keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop. Condition persists for more than 72 hours

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

  • Apply thoroughly to hands to cover all surfaces. Rub hands together until dry.

Other information

STORAGE AND HANDLING SECTION

  • Keep out of light, store at room temperature 59 - 86 degrees Farenheit

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, purified water USP

RECENT MAJOR CHANGES SECTION

Single wipe use. Apply thoroughly to hands to cover all surfaces. Rub hands together until dry.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Wipes Label ImageWipes Label Image230 mL NDC: 76830-501-07

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76830-501-072022-01-28C16284748780-1d6a99b39-c7b3-a426-e053-dadaa90af4c2ad530baa-1618-0d7b-e053-2995a90adc50

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76830-501-07Sanitizer Wipes230 mL in 1 PACKETLIQUID2301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76830-501SANITIZER WIPES (SANITIZING WIPES) LIQUID [ORGANIC FILLING SOLUTIONS, LLC]1Legacy NDC, 1 package rows20200821_ad530baa-1618-0d7b-e053-2995a90adc50.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76830-50176830-501-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
ad52ff6f-5364-8747-e053-2a95a90ac126ad530baa-1618-0d7b-e053-2995a90adc502020-08-20WarningsExact identifier
spl id: ad52ff6f-5364-8747-e053-2a95a90ac126
spl set id: ad530baa-1618-0d7b-e053-2995a90adc50

Reported adverse events (FAERS/openFDA)#

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