ZIVA WATER WIPES

Manufacturer
Ziva Wetwipes FZCo | Dirra USA
Effective date
2021-12-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:45:54

Label at a glance#

ProductZIVA WATER WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Label contents#

Full prescribing information#

Active Ingredient: 

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.01%

Direction for use

INDICATIONS & USAGE SECTION

For external use only. Open the flip top & peel back the front label slowly. Pull one wipe at a time. Gently cleanse your baby's skin using one or more wipes. Reseal pouch by firmly running thumb over label and close the flip top to prevent moisture loss.

Precautions:

WARNINGS SECTION

Do not apply to irritated or damaged skin. In case of gluteal erythema (redness of skin), contact your doctor or pharmacist. Keep in a cool place away from direct sunlight. Prevent contact with eyes. In case of irritation wash away with water immediately.

Other information

SPL UNCLASSIFIED SECTION

Store below 25°C 

Ingredients

INACTIVE INGREDIENT SECTION

Aqua, Pyrus Malus (apple) fruit extract, Benzalkonium Chloride.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81450-006-012023-01-30C16284748780-1f386c64a-0fa2-0266-e053-dadaa90a7c1aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81450-006-01ZIVA WATER WIPES100 in 1 PACKAGECLOTH1001
81450-006-01ZIVA WATER WIPES6.12 mL in 1 NOT APPLICABLECLOTH6.121

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81450-006ZIVA WATER WIPES (BENZALKONIUM CHLORIDE) CLOTH [ZIVA WETWIPES FZCO]1Legacy NDC, 2 package rows20211224_c93e05e6-0340-4caa-ba84-c15db210568f.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
81450-00681450-006-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
d3d75570-e81b-c783-e053-2a95a90a88f8c93e05e6-0340-4caa-ba84-c15db210568f2021-12-23WarningsExact identifier
spl id: d3d75570-e81b-c783-e053-2a95a90a88f8
spl set id: c93e05e6-0340-4caa-ba84-c15db210568f

Reported adverse events (FAERS/openFDA)#

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