1200 Wet Wipes

Manufacturer
D D Office Products, Inc.
Effective date
2020-07-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:38

Label at a glance#

Product1200 Wet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Storage and handling

• Store below 110°F (43°C). • May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.10%

Purpose

OTC - PURPOSE SECTION

Sanitizing

Use

INDICATIONS & USAGE SECTION

hand sanitizer to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only. 

Keep out of reach of eyes. If contact occurs, rinse thoroughly with water.

Do not use if you are allergic to any of the ingredients.

Discontinue use if irritation or redness develops, and if condition persists for more than 72 hours consult a physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children unless under adult supervision. 

If swallowed, get medical help

DOSAGE & ADMINISTRATION SECTION

Direction

Wet hands thoroughly with product and allow to dry without wiping.

Additional Information:

STORAGE AND HANDLING SECTION

• Store below 110°F (43°C).

• May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Sodium Carboxymethyl Lauryl Glucoside, Sodium PCA, Cocamide DEA, Citric Acid, Parfum / Fragrance, Ethyl glycerin, Vitamin E, Water, Aloe Essence Extract, Phenoxyethanol

SPL UNCLASSIFIED SECTION

Distributed by DD Office Products, Inc.

Los Angeles, CA | www.libertypp.com

Made in China

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038856benzalkonium Cl 0.1 % Medicated PadPSN1
1038856benzalkonium chloride 1 MG/ML Medicated PadSCD1
1038856benzalkonium chloride 0.1 % Medicated WipesSY1
1038856benzalkonium chloride 0.1 % Topical SwabSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77081-001-122022-01-28C16284748780-1d6a99b39-77c2-a426-e053-dadaa90af4c21200 WIPES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77081-001-121200 Wet Wipes3.5 mL in 1 PACKAGECLOTH3.51
77081-001-121200 Wet Wipes1200 in 1 BAGCLOTH12001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77081-0011200 WET WIPES (BENZALKONIUM CHLORIDE) CLOTH [D D OFFICE PRODUCTS, INC.]1Legacy NDC, 2 package rows20200717_9c8453eb-493a-4339-8ef8-77de738c6fc3.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77081-00177081-001-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
74e86c36-182c-4d0d-b460-9e1e54c3c3d19c8453eb-493a-4339-8ef8-77de738c6fc32020-07-13WarningsExact identifier
spl id: 74e86c36-182c-4d0d-b460-9e1e54c3c3d1
spl set id: 9c8453eb-493a-4339-8ef8-77de738c6fc3

Reported adverse events (FAERS/openFDA)#

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